A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260593



Internal ID20469811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75773938..75774001hg38UCSC Ensembl
chr14:76240281..76240344hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740429
Supporting Variants
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260593
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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