A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552087



Internal ID18753163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103117253..103117471hg38UCSC Ensembl
Outerchr14:103117193..103117524hg38UCSC Ensembl
Innerchr14:103583590..103583808hg19UCSC Ensembl
Outerchr14:103583530..103583861hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9750834
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552087
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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