A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983005



Internal ID21892348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233771003..233773340hg38UCSC Ensembl
chr1:233906749..233909086hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg382338
hg192338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983005
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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