A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602185



Internal ID16389594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32683032hg38UCSC Ensembl
Innerchr6:32455482..32650809hg19UCSC Ensembl
Innerchr6:32563460..32758787hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38195328
hg19195328
hg18195328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10489n54
Supporting Variantsnssv1054516
Samples
Known GenesHLA-DQA1, HLA-DQB1, 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)nsv602185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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