A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602756



Internal ID16390165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32644620..32660181hg38UCSC Ensembl
Innerchr6:32612397..32627958hg19UCSC Ensembl
Innerchr6:32720375..32735936hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3815562
hg1915562
hg1815562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10595n54
Supporting Variantsnssv1056673, nssv1056674
Samples
Known GenesHLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602756
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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