A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880761



Internal ID22655731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109417722..109417959hg38UCSC Ensembl
chr1:109960344..109960581hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363405
Samples
Known GenesPSMA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880761
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