A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015493



Internal ID21924836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114486938..114486993hg38UCSC Ensembl
chr9:117249218..117249273hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582211
Samples
Known GenesDFNB31
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015493
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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