CaSNP Project:

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Query Input

Please notice the genomic coordinate and annotation system for this database are based on GRCh37 human genome(UCSC hg19, Feb.2009 Assembly)

Genomic position: (gene name, refSeq ID, coordinate range or miRNA ID)

Genomic position:   

Examples: BRCA1, NM_017414, chr3:1-1000000, mir-137

Cancer type: (optional)



Caculate the frequency of copy number aberrations which are: (optional)

Greater Than:     and/or    Less Than:   

Examples: GT 2.2 (one-sided region), GT 2.2 and LT 1.8 (two-sided region), GT 1.8 and LT 2.2 (close region)