A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208487



Internal ID20775528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128574551..128575071hg38UCSC Ensembl
chr3:128293394..128293914hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366435
Supporting Variants
Samples
Known GenesC3orf27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208487
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