A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565196



Internal ID18766272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186292993..186293552hg38UCSC Ensembl
Outerchr4:186292788..186293653hg38UCSC Ensembl
Innerchr4:187214147..187214706hg19UCSC Ensembl
Outerchr4:187213942..187214807hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763943
Samples
Known GenesF11-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565196
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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