A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364970



Internal ID22590639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116320282..116320282hg38UCSC Ensembl
chr11:116190999..116190999hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974606
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364970
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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