A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696399



Internal ID120065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56616694..56648898hg38UCSC Ensembl
chr14:57083412..57115616hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3832205
hg1932205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504067
Supporting Variants
Samples
Known GenesTMEM260
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696399
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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