A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987122



Internal ID20554164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116841749..116842062hg38UCSC Ensembl
chr11:116712465..116712778hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468534
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.1213


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