A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057634



Internal ID15564134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33086269..33086898hg38UCSC Ensembl
Innerchr6:33054046..33054675hg19UCSC Ensembl
Innerchr6:33162024..33162653hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38630
hg19630
hg18630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602823
Supporting Variants
Samples
Known GenesHLA-DPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057634
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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