A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999526



Internal ID21908869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2145285..2146763hg38UCSC Ensembl
chr5:2145399..2146877hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556238
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999526
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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