A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993728



Internal ID20560768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58421758..58422255hg38UCSC Ensembl
chr11:58189231..58189728hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468604
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00046


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