A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994943



Internal ID21904286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12336586..12343095hg38UCSC Ensembl
chr4:12338210..12344719hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg386510
hg196510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994943
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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