A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763076



Internal ID18737322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:100195579..100195691hg38UCSC Ensembl
Outerchr4:100195554..100195707hg38UCSC Ensembl
Innerchr4:101116736..101116848hg19UCSC Ensembl
Outerchr4:101116711..101116864hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763076
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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