A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510066



Internal ID286696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75747564..75747747hg38UCSC Ensembl
chr14:76213907..76214090hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697929
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510066
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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