A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761109



Internal ID18735355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109384704..109386097hg38UCSC Ensembl
Outerchr3:109384407..109386133hg38UCSC Ensembl
Innerchr3:109103551..109104944hg19UCSC Ensembl
Outerchr3:109103254..109104980hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg381727
hg191727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562362
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761109
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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