A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10542n54



Internal ID22778437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32536098..32673970hg38UCSC Ensembl
chr6:32503875..32641747hg19UCSC Ensembl
chr6:32611853..32749725hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38137873
hg19137873
hg18137873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602535, nsv602491, nsv602557, nsv602506, nsv602530, nsv602516, nsv602470, nsv602525, nsv602518, nsv602484, nsv602555, nsv602558, nsv602495
Samples
Known GenesHLA-DQA1, HLA-DQB1, HLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10542n54
Frequency
Sample Size17421
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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