A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215892



Internal ID20782932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155871458..155879579hg38UCSC Ensembl
chr5:155298468..155306589hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg388122
hg198122
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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