A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10554n54



Internal ID22778449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32553420..32658151hg38UCSC Ensembl
chr6:32521197..32625928hg19UCSC Ensembl
chr6:32629175..32733906hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38104732
hg19104732
hg18104732
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602524, nsv602517, nsv602644, nsv602657
Samples
Known GenesHLA-DQA1, HLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10554n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss12
Observed Complex0
Frequencyn/a


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