A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10563n54



Internal ID22778458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32571614..32658309hg38UCSC Ensembl
chr6:32539391..32626086hg19UCSC Ensembl
chr6:32647369..32734064hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3886696
hg1986696
hg1886696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602582, nsv602583, nsv602643
Samples
Known GenesHLA-DQA1, HLA-DRB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10563n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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