A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984019



Internal ID21893362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31920257..31920331hg38UCSC Ensembl
chr1:32385858..32385932hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518918
Samples
Known GenesPTP4A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984019
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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