A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097843



Internal ID22007076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90412923..90412923hg38UCSC Ensembl
chr9:93175205..93175205hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097843
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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