A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983630



Internal ID21892973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26868338..26876219hg38UCSC Ensembl
chr1:27194829..27202710hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg387882
hg197882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983630
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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