A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670072



Internal ID9936177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32697770..32785283hg38UCSC Ensembl
Outerchr6:32697736..32785318hg38UCSC Ensembl
Innerchr6:32665547..32753060hg19UCSC Ensembl
Outerchr6:32665513..32753095hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3887583
hg1987583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6119513
SamplesHG00237
Known GenesHLA-DQA2, HLA-DQB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670072
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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