A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178417



Internal ID20745457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84508749..84517577hg38UCSC Ensembl
chr14:84975093..84983921hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg388829
hg198829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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