A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602516



Internal ID16389925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32553420..32656837hg38UCSC Ensembl
Innerchr6:32521197..32624614hg19UCSC Ensembl
Innerchr6:32629175..32732592hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38103418
hg19103418
hg18103418
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10542n54
Supporting Variantsnssv1055729, nssv1055730
Samples
Known GenesHLA-DQA1, HLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602516
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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