A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093381



Internal ID22002614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91510812..91510812hg38UCSC Ensembl
chr9:94273094..94273094hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587994
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093381
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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