A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178719



Internal ID20745759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85199558..85200374hg38UCSC Ensembl
chr14:85665902..85666718hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178719
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00044


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