A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698255



Internal ID121921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67242875..67251515hg38UCSC Ensembl
chr14:67709592..67718232hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg388641
hg198641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511917
Supporting Variants
Samples
Known GenesMPP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698255
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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