A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694397



Internal ID15084363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23080343..23183569hg38UCSC Ensembl
Innerchr8:22937856..23041082hg19UCSC Ensembl
Innerchr8:22993801..23097027hg18UCSC Ensembl
Innerchr8:22993801..23097027hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38103227
hg19103227
hg18103227
hg17103227
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520728
Supporting Variants
Samples
Known GenesLOC254896, LOC286059, TNFRSF10C, TNFRSF10D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694397
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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