A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192597



Internal ID20759637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34635877..34657674hg38UCSC Ensembl
chr14:35105083..35126880hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3821798
hg1921798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192597
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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