A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153025



Internal ID21415102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109356630..109361831hg38UCSC Ensembl
chr9:112118910..112124111hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385202
hg195202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595302
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153025
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