A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196766



Internal ID20763806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24239332..24551825hg38UCSC Ensembl
chr15:24484479..24796972hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38312494
hg19312494
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510778
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196766
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00494


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