A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981754



Internal ID21891097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171292090..171292413hg38UCSC Ensembl
chr1:171261229..171261552hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981754
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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