A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10503n54



Internal ID22778398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32487705..32563468hg38UCSC Ensembl
chr6:32455482..32531245hg19UCSC Ensembl
chr6:32563460..32639223hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3875764
hg1975764
hg1875764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602170, nsv602297, nsv602174, nsv602171, nsv602175, nsv602256, nsv602208, nsv602257, nsv602173, nsv602172
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)dgv10503n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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