A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750739



Internal ID18724985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94172519..94173532hg38UCSC Ensembl
Outerchr14:94172301..94173630hg38UCSC Ensembl
Innerchr14:94638856..94639869hg19UCSC Ensembl
Outerchr14:94638638..94639967hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381330
hg191330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551992
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750739
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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