A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992916



Internal ID20559956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79945100..79945940hg38UCSC Ensembl
chr11:79656143..79656983hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457043
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00059


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