A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210799



Internal ID20777839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94612793..94666681hg38UCSC Ensembl
chr3:94331637..94385525hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3853889
hg1953889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210799
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