A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696517



Internal ID120183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39170877..39171454hg38UCSC Ensembl
chr14:39640081..39640658hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696517
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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