A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614861



Internal ID21806908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124296765..124296765hg38UCSC Ensembl
chr11:124166661..124166661hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614861
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