A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750665



Internal ID18724911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87134163..87134590hg38UCSC Ensembl
Outerchr14:87134151..87134634hg38UCSC Ensembl
Innerchr14:87600507..87600934hg19UCSC Ensembl
Outerchr14:87600495..87600978hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551918
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750665
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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