A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013305



Internal ID21922648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97089608..97102989hg38UCSC Ensembl
chr9:99851890..99865271hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3813382
hg1913382
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013305
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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