A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479490



Internal ID21137043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75758339..75758870hg38UCSC Ensembl
chr14:76224682..76225213hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021152
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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