A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179202



Internal ID20746242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75819974..75820250hg38UCSC Ensembl
chr14:76286317..76286593hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486476
Supporting Variants
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179202
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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