A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981903



Internal ID21891246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162611247..162614304hg38UCSC Ensembl
chr1:162581037..162584094hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg383058
hg193058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981903
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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