A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602722



Internal ID16390131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32641154..32660651hg38UCSC Ensembl
Innerchr6:32608931..32628428hg19UCSC Ensembl
Innerchr6:32716909..32736406hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3819498
hg1919498
hg1819498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10591n54
Supporting Variantsnssv1056545
Samples
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)nsv602722
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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