A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693415



Internal ID15083381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8780666..8816277hg38UCSC Ensembl
Innerchr3:8822352..8857963hg19UCSC Ensembl
Innerchr3:8797352..8832963hg18UCSC Ensembl
Innerchr3:8797352..8832963hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3835612
hg1935612
hg1835612
hg1735612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517310
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693415
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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