A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862727



Internal ID22637662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75924064..75925907hg38UCSC Ensembl
chr14:76390407..76392250hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381844
hg191844
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453189
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862727
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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