A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546996



Internal ID18748072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125167490..125170774hg38UCSC Ensembl
Outerchr10:125167341..125170874hg38UCSC Ensembl
Innerchr10:126856059..126859343hg19UCSC Ensembl
Outerchr10:126855910..126859443hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383534
hg193534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745743
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546996
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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