A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760483



Internal ID18712078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23056273..23105040hg38UCSC Ensembl
Innerchr8:22913786..22962553hg19UCSC Ensembl
Innerchr8:22969731..23018498hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3848768
hg1948768
hg1848768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015967
Supporting Variants
Samples
Known GenesLOC254896, LOC286059, TNFRSF10B, TNFRSF10C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3760483
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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