A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10523n54



Internal ID22778418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32505399..32597007hg38UCSC Ensembl
chr6:32473176..32564784hg19UCSC Ensembl
chr6:32581154..32672762hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3891609
hg1991609
hg1891609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602363, nsv602404, nsv602373, nsv602419, nsv602393, nsv602365, nsv602390, nsv602374, nsv602364, nsv602392, nsv602372, nsv602389, nsv602391
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)dgv10523n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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