A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10595n54



Internal ID22778490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32644620..32660181hg38UCSC Ensembl
chr6:32612397..32627958hg19UCSC Ensembl
chr6:32720375..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 Variants
Supporting Variantsnsv602754, nsv602756, nsv602771, nsv602762, nsv602753, nsv602769, nsv602761, nsv602760, nsv602770
Samples
Known GenesHLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10595n54
Frequency
Sample Size17421
Observed Gain29
Observed Loss0
Observed Complex0
Frequencyn/a


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