A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698340



Internal ID122006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102261332..102267549hg38UCSC Ensembl
chr14:102727669..102733886hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg386218
hg196218
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5564123
Supporting Variants
Samples
Known GenesMOK
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698340
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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