A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749962



Internal ID18724208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21551207..21555382hg38UCSC Ensembl
Outerchr14:21551176..21555404hg38UCSC Ensembl
Innerchr14:22019355..22023513hg19UCSC Ensembl
Outerchr14:22019324..22023535hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg384229
hg194212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749962
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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