A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546458



Internal ID18747534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68452145..68453308hg38UCSC Ensembl
Outerchr10:68452126..68453519hg38UCSC Ensembl
Innerchr10:70211902..70213065hg19UCSC Ensembl
Outerchr10:70211883..70213276hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381394
hg191394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745205
Samples
Known GenesDNA2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546458
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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