A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611620



Internal ID16399029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:82407106..82577509hg38UCSC Ensembl
Innerchr8:83319341..83489744hg19UCSC Ensembl
Innerchr8:83481896..83652299hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38170404
hg19170404
hg18170404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12214n54
Supporting Variantsnssv1117317
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611620
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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