A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602186



Internal ID16389595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32683279hg38UCSC Ensembl
Innerchr6:32455482..32651056hg19UCSC Ensembl
Innerchr6:32563460..32759034hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38195575
hg19195575
hg18195575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10489n54
Supporting Variantsnssv1054517
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)nsv602186
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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