A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579222



Internal ID21527699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141942827..141942960hg38UCSC Ensembl
chr3:141661669..141661802hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131593
SamplesHG00733
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579222
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