A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750772



Internal ID18725018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98308201..98308508hg38UCSC Ensembl
Outerchr14:98308120..98308555hg38UCSC Ensembl
Innerchr14:98774538..98774845hg19UCSC Ensembl
Outerchr14:98774457..98774892hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552025
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750772
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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