A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745112



Internal ID18372672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58330394..58334760hg38UCSC Ensembl
Outerchr10:58329741..58335240hg38UCSC Ensembl
Innerchr10:60090154..60094520hg19UCSC Ensembl
Outerchr10:60089501..60095000hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546365
Supporting Variants
Samples
Known GenesUBE2D1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745112
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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