A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601507



Internal ID16388916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31269809..31372067hg38UCSC Ensembl
Innerchr6:31237586..31339844hg19UCSC Ensembl
Innerchr6:31345565..31447823hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38102259
hg19102259
hg18102259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10375n54
Supporting Variantsnssv1052351
Samples
Known GenesHLA-B, HLA-C, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601507
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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