A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749967



Internal ID18377527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22078321..22493013hg38UCSC Ensembl
Outerchr14:22006762..22515018hg38UCSC Ensembl
Innerchr14:22546582..22962000hg19UCSC Ensembl
Outerchr14:22475001..22984000hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38508257
hg19509000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749967
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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