A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760675



Internal ID18734921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57695321..57695507hg38UCSC Ensembl
Outerchr3:57695283..57695523hg38UCSC Ensembl
Innerchr3:57681048..57681234hg19UCSC Ensembl
Outerchr3:57681010..57681250hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561928
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760675
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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