A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153716



Internal ID15874667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65918786..66111599hg38UCSC Ensembl
Innerchr6:66628679..66821492hg19UCSC Ensembl
Innerchr6:66685400..66878213hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38192814
hg19192814
hg18192814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603475
Supporting Variants
SamplesHGDP00571
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153716
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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