A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487920



Internal ID21145473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75746714..75899535hg38UCSC Ensembl
chr14:76213057..76365878hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38152822
hg19152822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021151
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487920
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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