A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194080



Internal ID20761120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85332787..85383663hg38UCSC Ensembl
chr14:85799131..85850007hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3850877
hg1950877
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194080
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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