A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544668



Internal ID18745744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22960089..22962524hg38UCSC Ensembl
Outerchr9:22960057..22962559hg38UCSC Ensembl
Innerchr9:22960088..22962523hg19UCSC Ensembl
Outerchr9:22960056..22962558hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382503
hg192503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743415
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544668
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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