A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004058



Internal ID21913401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35120060..35130023hg38UCSC Ensembl
chr9:35120057..35130020hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg389964
hg199964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004058
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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