A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020045



Internal ID21929388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85746677..85852545hg38UCSC Ensembl
chr9:88361592..88467460hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38105869
hg19105869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579763
Samples
Known GenesLOC389765
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020045
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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