A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081336



Internal ID21990569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125190786..125190786hg38UCSC Ensembl
chr12:125675332..125675332hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081336
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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