A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546756



Internal ID18747832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101634379..101635329hg38UCSC Ensembl
Outerchr10:101634196..101635451hg38UCSC Ensembl
Innerchr10:103394136..103395086hg19UCSC Ensembl
Outerchr10:103393953..103395208hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381256
hg191256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745503
Samples
Known GenesFBXW4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546756
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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