A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602518



Internal ID16389927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32553420..32673970hg38UCSC Ensembl
Innerchr6:32521197..32641747hg19UCSC Ensembl
Innerchr6:32629175..32749725hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38120551
hg19120551
hg18120551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10542n54
Supporting Variantsnssv1055737
Samples
Known GenesHLA-DQA1, HLA-DQB1, HLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602518
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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