A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749982



Internal ID18724228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22864213..22864390hg38UCSC Ensembl
Outerchr14:22864206..22864417hg38UCSC Ensembl
Innerchr14:23333422..23333599hg19UCSC Ensembl
Outerchr14:23333415..23333626hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749982
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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