A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743927



Internal ID18718173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98024294..98027014hg38UCSC Ensembl
Outerchr9:98024250..98027140hg38UCSC Ensembl
Innerchr9:100786576..100789296hg19UCSC Ensembl
Outerchr9:100786532..100789422hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382891
hg192891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545180
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743927
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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