A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980592



Internal ID21889935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109424932..109425021hg38UCSC Ensembl
chr1:109967554..109967643hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522162
Samples
Known GenesPSMA5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980592
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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