A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584885



Internal ID21776928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34935572..34938915hg38UCSC Ensembl
chr9:34935569..34938912hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383344
hg193344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584885
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