A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192024



Internal ID20759064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106260351..106730825hg38UCSC Ensembl
chr14:106716948..107174928hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38470475
hg19457981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498418
Supporting Variants
Samples
Known GenesLINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192024
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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