A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10506n54



Internal ID22778401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32487705..32603062hg38UCSC Ensembl
chr6:32455482..32570839hg19UCSC Ensembl
chr6:32563460..32678817hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38115358
hg19115358
hg18115358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602271, nsv602270, nsv602209, nsv602268, nsv602266, nsv602261, nsv602212, nsv602213, nsv602326, nsv602317, nsv602325, nsv602179, nsv602262, nsv602258, nsv602218, nsv602194, nsv602214, nsv602219, nsv602210, nsv602264, nsv602263, nsv602299, nsv602211, nsv602233, nsv602315, nsv602180, nsv602220, nsv602181, nsv602269, nsv602260, nsv602177, nsv602265, nsv602215, nsv602259, nsv602298, nsv602192, nsv602308, nsv602178, nsv602272, nsv602193
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)dgv10506n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss154
Observed Complex0
Frequencyn/a


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