A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597080



Internal ID21789123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34674845..34674845hg38UCSC Ensembl
chr11:34696392..34696392hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597080
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