A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587175



Internal ID21779218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111387151..111387151hg38UCSC Ensembl
chr9:114149431..114149431hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082120
Supporting Variants
Samples
Known GenesKIAA0368
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587175
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