A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766299



Internal ID18740545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32489895..32533435hg38UCSC Ensembl
Outerchr6:32483574..32544223hg38UCSC Ensembl
Innerchr6:32457672..32501212hg19UCSC Ensembl
Outerchr6:32451351..32512000hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3860650
hg1960650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567552
Supporting Variants
Samples
Known GenesHLA-DRB5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766299
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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