A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602691



Internal ID16390100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32601914..32659937hg38UCSC Ensembl
Innerchr6:32569691..32627714hg19UCSC Ensembl
Innerchr6:32677669..32735692hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3858024
hg1958024
hg1858024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10572n54
Supporting Variantsnssv1154738
SamplesHGDP00066
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)nsv602691
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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