A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699357



Internal ID123023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77423072..77423123hg38UCSC Ensembl
chr14:77889415..77889466hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699357
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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