A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743887



Internal ID18718133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93968088..93968311hg38UCSC Ensembl
Outerchr9:93968030..93968350hg38UCSC Ensembl
Innerchr9:96730370..96730593hg19UCSC Ensembl
Outerchr9:96730312..96730632hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545140
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743887
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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