A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186943



Internal ID20753983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9622101..9623500hg38UCSC Ensembl
chr11:9643648..9645047hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447737
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186943
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.07682


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