A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088406



Internal ID21997639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75748281..75748281hg38UCSC Ensembl
chr14:76214624..76214624hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382417
hg192417
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615565
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088406
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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