A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602704



Internal ID16390113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32625121..32644620hg38UCSC Ensembl
Innerchr6:32592898..32612397hg19UCSC Ensembl
Innerchr6:32700876..32720375hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3819500
hg1919500
hg1819500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10585n54
Supporting Variantsnssv1056485
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602704
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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