A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191803



Internal ID20758843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76633173..76637228hg38UCSC Ensembl
chr14:77099516..77103571hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384056
hg194056
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191803
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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