A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177627



Internal ID20744667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50767601..50821300hg38UCSC Ensembl
chr11:50726772..50780471hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3853700
hg1953700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459046
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177627
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00575


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