A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602531



Internal ID16389940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32554612..32562421hg38UCSC Ensembl
Innerchr6:32522389..32530198hg19UCSC Ensembl
Innerchr6:32630367..32638176hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg387810
hg197810
hg187810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055796, nssv1055797, nssv1055798
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602531
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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