A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482832



Internal ID21140385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75924124..75926293hg38UCSC Ensembl
chr14:76390467..76392636hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382170
hg192170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021162
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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