A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697935



Internal ID121601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75849304..75894573hg38UCSC Ensembl
chr14:76315647..76360916hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3845270
hg1945270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500315
Supporting Variants
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697935
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer