A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211194



Internal ID20778234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37938601..37961700hg38UCSC Ensembl
chr3:37980092..38003191hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3823100
hg1923100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367292
Supporting Variants
Samples
Known GenesCTDSPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211194
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