A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985291



Internal ID21894634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10627546..10704818hg38UCSC Ensembl
chr2:10767672..10844944hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3877273
hg1977273
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525396
Samples
Known GenesNOL10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985291
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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