A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563481



Internal ID18764557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17304733..17305813hg38UCSC Ensembl
Outerchr4:17304719..17305816hg38UCSC Ensembl
Innerchr4:17306356..17307436hg19UCSC Ensembl
Outerchr4:17306342..17307439hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg381098
hg191098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762228
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563481
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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