A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695925



Internal ID15085891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:86220282..86237742hg38UCSC Ensembl
Innerchr8:87232511..87249971hg19UCSC Ensembl
Innerchr8:87301627..87319087hg18UCSC Ensembl
Innerchr8:87301627..87319087hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3817461
hg1917461
hg1817461
hg1717461
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519507
Supporting Variants
Samples
Known GenesSLC7A13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695925
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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