A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209726



Internal ID20776767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153362201..153383200hg38UCSC Ensembl
chr3:153079990..153100989hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3821000
hg1921000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358791
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209726
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00051


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