A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086797



Internal ID21996030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60575359..60575359hg38UCSC Ensembl
chr9_gl000199_random:56801..56801hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086797
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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