A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602342



Internal ID16389751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32501480..32658151hg38UCSC Ensembl
Innerchr6:32469257..32625928hg19UCSC Ensembl
Innerchr6:32577235..32733906hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38156672
hg19156672
hg18156672
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10519n54
Supporting Variantsnssv1055175, nssv1055176, nssv1055174
Samples
Known GenesHLA-DQA1, HLA-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)nsv602342
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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