A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189918



Internal ID20756958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103824131..103878033hg38UCSC Ensembl
chr14:104290468..104344370hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3853903
hg1953903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497976
Supporting Variants
Samples
Known GenesLINC00637, PPP1R13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189918
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer