A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999423



Internal ID21908766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:29316573..29576405hg38UCSC Ensembl
chr5:29316680..29576512hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38259833
hg19259833
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543557
Samples
Known GenesLOC101929681
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999423
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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