A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696774



Internal ID120440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65160993..65161122hg38UCSC Ensembl
chr14:65627711..65627840hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505006
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696774
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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