A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162465



Internal ID21463617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79413243..79418530hg38UCSC Ensembl
chr9:82028158..82033445hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg385288
hg195288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602647
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162465
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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