A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891756



Internal ID22666798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148882662..148882737hg38UCSC Ensembl
chr3:148600449..148600524hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427800
Samples
Known GenesCPA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891756
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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