A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749832



Internal ID18724078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110907085..110907296hg38UCSC Ensembl
Outerchr13:110907035..110907332hg38UCSC Ensembl
Innerchr13:111559432..111559643hg19UCSC Ensembl
Outerchr13:111559382..111559679hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551085
Supporting Variants
Samples
Known GenesANKRD10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749832
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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