A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999735



Internal ID21909078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42828451..42959011hg38UCSC Ensembl
chr5:42828553..42959113hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38130561
hg19130561
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999735
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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