A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096359



Internal ID21276824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:51318032..51321607hg38UCSC Ensembl
Innerchr16:51351943..51355518hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg383576
hg193576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112356
Supporting Variants
Samplessample242
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096359
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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