A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983159



Internal ID21892502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2435934..2436472hg38UCSC Ensembl
chr1:2367373..2367911hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983159
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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