A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10491n54



Internal ID22778386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32465982..32565053hg38UCSC Ensembl
chr6:32433759..32532830hg19UCSC Ensembl
chr6:32541737..32640808hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3899072
hg1999072
hg1899072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602133, nsv602134, nsv602152, nsv602128
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)dgv10491n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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