A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096346



Internal ID21276385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70798278..71024875hg38UCSC Ensembl
Innerchr16:70832181..71058778hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38226598
hg19226598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116173
Supporting Variants
Samplessample235
Known GenesHYDIN, VAC14
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096346
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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