A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093048



Internal ID22002281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92473119..92473119hg38UCSC Ensembl
chr12:92866895..92866895hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093048
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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