A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699246



Internal ID122912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73857179..73861177hg38UCSC Ensembl
chr14:74323882..74327880hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg383999
hg193999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511814
Supporting Variants
Samples
Known GenesPTGR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699246
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002185


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