A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563778



Internal ID18764854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42704388..42706983hg38UCSC Ensembl
Outerchr4:42703962..42707511hg38UCSC Ensembl
Innerchr4:42706405..42709000hg19UCSC Ensembl
Outerchr4:42705979..42709528hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg383550
hg193550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762525
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563778
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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