A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081826



Internal ID21991059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60573490..60573490hg38UCSC Ensembl
chr9_gl000199_random:54932..54932hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081826
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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