A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600627



Internal ID21792674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123734765..123734765hg38UCSC Ensembl
chr11:123605473..123605473hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096589
Supporting Variants
Samples
Known GenesZNF202
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600627
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