A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191925



Internal ID20758965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10522685..10535333hg38UCSC Ensembl
chr11:10544232..10556880hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3812649
hg1912649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450233
Supporting Variants
Samples
Known GenesRNF141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191925
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