A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209746



Internal ID20776787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155761843..155795690hg38UCSC Ensembl
chr3:155479632..155513479hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3833848
hg1933848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374328
Supporting Variants
Samples
Known GenesC3orf33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209746
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00535


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