A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602334



Internal ID16389743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32501123..32658151hg38UCSC Ensembl
Innerchr6:32468900..32625928hg19UCSC Ensembl
Innerchr6:32576878..32733906hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38157029
hg19157029
hg18157029
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10519n54
Supporting Variantsnssv1055153, nssv1055155, nssv1055154
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)nsv602334
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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