A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055571



Internal ID15908757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32529135..32542208hg38UCSC Ensembl
Innerchr6:32496912..32509985hg19UCSC Ensembl
Innerchr6:32604890..32617963hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3813074
hg1913074
hg1813074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602427
Supporting Variants
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055571
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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