A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182911



Internal ID20749951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113214981..113215721hg38UCSC Ensembl
chr13:113869295..113870035hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487681
Supporting Variants
Samples
Known GenesCUL4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182911
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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