A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098114



Internal ID22007347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135518668..135518668hg38UCSC Ensembl
chr9:138410514..138410514hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098114
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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