A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000964



Internal ID21910307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114542379..114542442hg38UCSC Ensembl
chr9:117304659..117304722hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000964
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