A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545828



Internal ID18746904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5847624..5850537hg38UCSC Ensembl
Outerchr10:5847275..5851037hg38UCSC Ensembl
Innerchr10:5889587..5892500hg19UCSC Ensembl
Outerchr10:5889238..5893000hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383763
hg193763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744575
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545828
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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