A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588524



Internal ID21780567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87057924..87058782hg38UCSC Ensembl
chr9:89672839..89673697hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019692
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588524
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