A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196406



Internal ID20763446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75469256..75636209hg38UCSC Ensembl
chr14:75935959..76102552hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38166954
hg19166594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488919
Supporting Variants
Samples
Known GenesBATF, FLVCR2, JDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196406
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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