A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897660



Internal ID22672765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73522740..73523330hg38UCSC Ensembl
chr3:73571891..73572481hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411069
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897660
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