A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992583



Internal ID20559623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66722327..66760677hg38UCSC Ensembl
chr11:66489798..66528148hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3838351
hg1938351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460961
Supporting Variants
Samples
Known GenesC11orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992583
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