A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179844



Internal ID20746884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57402112..57402528hg38UCSC Ensembl
chr11:57169585..57170001hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459451
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179844
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