A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10531n54



Internal ID22778426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32524531..32564146hg38UCSC Ensembl
chr6:32492308..32531923hg19UCSC Ensembl
chr6:32600286..32639901hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3839616
hg1939616
hg1839616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602431, nsv602418, nsv602440, nsv602471
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10531n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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