A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136859



Internal ID21487517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145705971..145707002hg38UCSC Ensembl
chr3:145423758..145424789hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381032
hg191032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572721
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136859
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