A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750532



Internal ID18724778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76347462..76347837hg38UCSC Ensembl
Outerchr14:76347378..76347913hg38UCSC Ensembl
Innerchr14:76813805..76814180hg19UCSC Ensembl
Outerchr14:76813721..76814256hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750532
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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