A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743762



Internal ID18718008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:82315730..82317505hg38UCSC Ensembl
Outerchr9:82315673..82317561hg38UCSC Ensembl
Innerchr9:84930645..84932420hg19UCSC Ensembl
Outerchr9:84930588..84932476hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381889
hg191889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545015
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743762
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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