A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10498n54



Internal ID22778393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32487705..32519392hg38UCSC Ensembl
chr6:32455482..32487169hg19UCSC Ensembl
chr6:32563460..32595147hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3831688
hg1931688
hg1831688
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602245, nsv602158, nsv602227, nsv602247, nsv602199
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10498n54
Frequency
Sample Size17421
Observed Gain14
Observed Loss63
Observed Complex0
Frequencyn/a


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