A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602758



Internal ID16390167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32644620..32811865hg38UCSC Ensembl
Innerchr6:32612397..32779642hg19UCSC Ensembl
Innerchr6:32720375..32887620hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38167246
hg19167246
hg18167246
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1056677, nssv1056679, nssv1056678, nssv1056676
Samples
Known GenesHLA-DQA2, HLA-DQB1, HLA-DQB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602758
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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