A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156586



Internal ID15874270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10678316..10710120hg38UCSC Ensembl
Innerchr8:10535826..10567630hg19UCSC Ensembl
Innerchr8:10573236..10605040hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3831805
hg1931805
hg1831805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610272
Supporting Variants
SamplesHGDP00515
Known GenesC8orf74
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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