A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098433



Internal ID21267675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4519406..4527626hg38UCSC Ensembl
Innerchr16:4569407..4577627hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388221
hg198221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113278
Supporting Variants
Samplessample116
Known GenesCDIP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098433
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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