A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984262



Internal ID21893605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46332789..46337762hg38UCSC Ensembl
chr1:46798461..46803434hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg384974
hg194974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984262
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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