A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209626



Internal ID20776666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139801771..140232097hg38UCSC Ensembl
chr3:139520613..139950939hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38430327
hg19430327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373152
Supporting Variants
Samples
Known GenesCLSTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209626
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