A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750702



Internal ID18724948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90525413..90525931hg38UCSC Ensembl
Outerchr14:90525339..90526053hg38UCSC Ensembl
Innerchr14:90991757..90992275hg19UCSC Ensembl
Outerchr14:90991683..90992397hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750702
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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