A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121834



Internal ID21401775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120499593..120500178hg38UCSC Ensembl
chr3:120218440..120219025hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575360
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121834
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