A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698843



Internal ID122509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101305320..101310966hg38UCSC Ensembl
chr14:101771657..101777303hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg385647
hg195647
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698843
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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