A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546910



Internal ID18747986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:117874780..117875088hg38UCSC Ensembl
Outerchr10:117874721..117875154hg38UCSC Ensembl
Innerchr10:119634291..119634599hg19UCSC Ensembl
Outerchr10:119634232..119634665hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745657
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546910
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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