A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184478



Internal ID20751518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106358301..106883700hg38UCSC Ensembl
chr14:106814230..107289540hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38525400
hg19475311
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502970
Supporting Variants
Samples
Known GenesLINC00221
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184478
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00175


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