A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696228



Internal ID119894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52308604..52339517hg38UCSC Ensembl
chr14:52775322..52806235hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3830914
hg1930914
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559453
Supporting Variants
Samples
Known GenesPTGER2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696228
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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