A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984900



Internal ID21894243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65874190..65875983hg38UCSC Ensembl
chr1:66339873..66341666hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381794
hg191794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523490
Samples
Known GenesPDE4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984900
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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