A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10501n54



Internal ID22778396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32487705..32534102hg38UCSC Ensembl
chr6:32455482..32501879hg19UCSC Ensembl
chr6:32563460..32609857hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3846398
hg1946398
hg1846398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602161, nsv602251, nsv602162, nsv602160, nsv602191, nsv602253, nsv602293, nsv602252, nsv602203, nsv602307, nsv602296
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10501n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss81
Observed Complex0
Frequencyn/a


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