A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981555



Internal ID21890898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160293710..160293871hg38UCSC Ensembl
chr1:160263500..160263661hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526719
Samples
Known GenesCOPA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981555
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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