A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3553906



Internal ID18408296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89579859..89580195hg38UCSC Ensembl
Outerchr16:89579760..89580248hg38UCSC Ensembl
Innerchr16:89646267..89646603hg19UCSC Ensembl
Outerchr16:89646168..89646656hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9752653
Samples
Known GenesCPNE7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3553906
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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