A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957794



Internal ID22732893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153906965..153906965hg38UCSC Ensembl
chr3:153624754..153624754hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957794
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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