A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761800



Internal ID18736046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188015361..188016877hg38UCSC Ensembl
Outerchr3:188015019..188017087hg38UCSC Ensembl
Innerchr3:187733149..187734665hg19UCSC Ensembl
Outerchr3:187732807..187734875hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg382069
hg192069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761800
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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