A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762467



Internal ID18736713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:37764683..37764982hg38UCSC Ensembl
Outerchr4:37764640..37765004hg38UCSC Ensembl
Innerchr4:37766305..37766604hg19UCSC Ensembl
Outerchr4:37766262..37766626hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762467
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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