A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707980



Internal ID131646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14245267..14245277hg38UCSC Ensembl
chr16:14339124..14339134hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3811
hg1911
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554796
Supporting Variants
Samples
Known GenesMKL2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707980
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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