A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983840



Internal ID21893183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32517302..32522282hg38UCSC Ensembl
chr1:32982903..32987883hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg384981
hg194981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983840
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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