A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442874



Internal ID21100427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18725544..18727002hg38UCSC Ensembl
chr11:18747091..18748549hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381459
hg191459
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196364
Samples
Known GenesIGSF22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442874
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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