A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698486



Internal ID122152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104764084..104764084hg38UCSC Ensembl
chr14:105230421..105230421hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540116
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698486
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.200131


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