A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453189



Internal ID22511063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75924064..75925907hg38UCSC Ensembl
chr14:76390407..76392250hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381844
hg191844
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862727
Supporting Variants
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453189
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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