A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697941



Internal ID121607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75924149..75926228hg38UCSC Ensembl
chr14:76390492..76392571hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382080
hg192080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494177
Supporting Variants
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697941
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01015


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