A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580101



Internal ID21772144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19860131..19860131hg38UCSC Ensembl
chr11:19881677..19881677hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092688
Supporting Variants
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580101
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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