A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1056584



Internal ID15909770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32641349..32658760hg38UCSC Ensembl
Innerchr6:32609126..32626537hg19UCSC Ensembl
Innerchr6:32717104..32734515hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3817412
hg1917412
hg1817412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602727
Supporting Variants
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1056584
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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