A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606584



Internal ID21554889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145032515..145032515hg38UCSC Ensembl
chr3:144751357..144751357hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135200
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606584
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