A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703969



Internal ID15093935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:38747015..38801421hg38UCSC Ensembl
Innerchr3:38788506..38842912hg19UCSC Ensembl
Innerchr3:38763510..38817916hg18UCSC Ensembl
Innerchr3:38763510..38817916hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3854407
hg1954407
hg1854407
hg1754407
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527515
Supporting Variants
Samples
Known GenesSCN10A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703969
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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