A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695840



Internal ID119506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:33640895..33640971hg38UCSC Ensembl
chr14:34110101..34110177hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494296
Supporting Variants
Samples
Known GenesNPAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695840
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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