A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896196



Internal ID22671285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140902265..140903515hg38UCSC Ensembl
chr3:140621107..140622357hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381251
hg191251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896196
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