A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749767



Internal ID18724013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104583626..104586383hg38UCSC Ensembl
Outerchr13:104583404..104586453hg38UCSC Ensembl
Innerchr13:105235977..105238734hg19UCSC Ensembl
Outerchr13:105235755..105238804hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg383050
hg193050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551020
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749767
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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