A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739568



Internal ID18367128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163497969..163522383hg38UCSC Ensembl
Outerchr6:163496159..163523134hg38UCSC Ensembl
Innerchr6:163919001..163943415hg19UCSC Ensembl
Outerchr6:163917191..163944166hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3826976
hg1926976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540821
Supporting Variants
Samples
Known GenesQKI
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739568
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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