A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697708



Internal ID15087674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39458653..39474994hg38UCSC Ensembl
Innerchr3:39500144..39516485hg19UCSC Ensembl
Innerchr3:39475148..39491489hg18UCSC Ensembl
Innerchr3:39475148..39491489hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3816342
hg1916342
hg1816342
hg1716342
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520957
Supporting Variants
Samples
Known GenesMOBP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697708
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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