A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053956



Internal ID15907142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32476099..32592608hg38UCSC Ensembl
Innerchr6:32443876..32560385hg19UCSC Ensembl
Innerchr6:32551854..32668363hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38116510
hg19116510
hg18116510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602146
Supporting Variants
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053956
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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