A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9748962



Internal ID18723208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26510514..26511078hg38UCSC Ensembl
Outerchr13:26510483..26511104hg38UCSC Ensembl
Innerchr13:27084651..27085215hg19UCSC Ensembl
Outerchr13:27084620..27085241hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3550215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9748962
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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