A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761379



Internal ID18735625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140902608..140903508hg38UCSC Ensembl
Outerchr3:140902426..140903685hg38UCSC Ensembl
Innerchr3:140621450..140622350hg19UCSC Ensembl
Outerchr3:140621268..140622527hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761379
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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