A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762619



Internal ID18736865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:55132407..55132643hg38UCSC Ensembl
Outerchr4:55132336..55132739hg38UCSC Ensembl
Innerchr4:55998574..55998810hg19UCSC Ensembl
Outerchr4:55998503..55998906hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762619
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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