A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188643



Internal ID20755683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65689101..65724700hg38UCSC Ensembl
chr14:66155819..66191418hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3835600
hg1935600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477485
Supporting Variants
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188643
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00061


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