A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567589



Internal ID18768665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33125654..33125958hg38UCSC Ensembl
Outerchr6:33125577..33126010hg38UCSC Ensembl
Innerchr6:33093431..33093735hg19UCSC Ensembl
Outerchr6:33093354..33093787hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766336
Samples
Known GenesHLA-DPB2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567589
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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