A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984135



Internal ID21893478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40969801..40973082hg38UCSC Ensembl
chr1:41435473..41438754hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg383282
hg193282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984135
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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