A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055721



Internal ID15908907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32553306..32565053hg38UCSC Ensembl
Innerchr6:32521083..32532830hg19UCSC Ensembl
Innerchr6:32629061..32640808hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3811748
hg1911748
hg1811748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602512
Supporting Variants
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055721
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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