A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057626



Internal ID15910812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33061660..33065245hg38UCSC Ensembl
Innerchr6:33029437..33033022hg19UCSC Ensembl
Innerchr6:33137415..33141000hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383586
hg193586
hg183586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602822
Supporting Variants
Samples
Known GenesHLA-DPA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057626
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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