A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10505n54



Internal ID22778400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32487705..32601910hg38UCSC Ensembl
chr6:32455482..32569687hg19UCSC Ensembl
chr6:32563460..32677665hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38114206
hg19114206
hg18114206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602234, nsv602306, nsv602236, nsv602217, nsv602235, nsv602232, nsv602183, nsv602231, nsv602216, nsv602344, nsv602300, nsv602230
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)dgv10505n54
Frequency
Sample Size17421
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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