A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573834



Internal ID21522242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179850078..179850272hg38UCSC Ensembl
chr1:179819213..179819407hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061424
SamplesNA19239
Known GenesTOR1AIP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573834
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