A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025279



Internal ID18767811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23079697..23182344hg38UCSC Ensembl
Innerchr8:22937210..23039857hg19UCSC Ensembl
Innerchr8:22993155..23095802hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38102648
hg19102648
hg18102648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760484
Samples
Known GenesLOC254896, LOC286059, TNFRSF10C, TNFRSF10D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025279
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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