A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607232



Internal ID21555537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155298032..155298032hg38UCSC Ensembl
chr3:155015821..155015821hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135721
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607232
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