A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622358



Internal ID21570663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13331032..13331032hg38UCSC Ensembl
chr3:13372532..13372532hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120225
SamplesNA12878
Known GenesNUP210
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622358
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer