A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685034



Internal ID21206890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89224968..89224968hg38UCSC Ensembl
chr16:89291376..89291376hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796428
Supporting Variants
Samples
Known GenesZNF778
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685034
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.589286


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