A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986630



Internal ID20553670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118829913..118832205hg38UCSC Ensembl
chr11:118700622..118702914hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382293
hg192293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462764
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986630
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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