A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981823



Internal ID21891166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170701163..170701370hg38UCSC Ensembl
chr1:170670304..170670511hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519979
Samples
Known GenesPRRX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981823
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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