A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099289



Internal ID21275962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4008912..4012767hg38UCSC Ensembl
Innerchr16:4058913..4062768hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383856
hg193856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111607
Supporting Variants
Samplessample230
Known GenesADCY9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099289
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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