A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196752



Internal ID20763792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55568146..55629471hg38UCSC Ensembl
chr14:56034864..56096189hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3861326
hg1961326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493627
Supporting Variants
Samples
Known GenesKTN1, KTN1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196752
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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