A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656493



Internal ID15046459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100635680..100714748hg38UCSC Ensembl
Innerchr3:100354524..100433592hg19UCSC Ensembl
Innerchr3:101837214..101916282hg18UCSC Ensembl
Innerchr3:101837214..101916282hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3879069
hg1979069
hg1879069
hg1779069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516418
Supporting Variants
Samples
Known GenesGPR128, TFG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656493
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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