A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10492n54



Internal ID22778387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32472704..32621031hg38UCSC Ensembl
chr6:32440481..32588808hg19UCSC Ensembl
chr6:32548459..32696786hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38148328
hg19148328
hg18148328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602345, nsv602146, nsv602142, nsv602141, nsv602148, nsv602143, nsv602130, nsv602140, nsv602145
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10492n54
Frequency
Sample Size17421
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer