A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749908



Internal ID18724154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113737316..113737427hg38UCSC Ensembl
Outerchr13:113737311..113737453hg38UCSC Ensembl
Innerchr13:114440289..114440400hg19UCSC Ensembl
Outerchr13:114440284..114440426hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749908
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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