A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602697



Internal ID16390106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32622686..32687441hg38UCSC Ensembl
Innerchr6:32590463..32655218hg19UCSC Ensembl
Innerchr6:32698441..32763196hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3864756
hg1964756
hg1864756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10582n54
Supporting Variantsnssv1154741
SamplesHGDP00546
Known GenesHLA-DQA1, HLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602697
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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