A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708818



Internal ID132484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89319837..89335909hg38UCSC Ensembl
chr16:89386245..89402317hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3816073
hg1916073
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532486
Supporting Variants
Samples
Known GenesANKRD11, LOC100287036
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708818
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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