A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080999



Internal ID21990232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125067027..125067027hg38UCSC Ensembl
chr12:125551573..125551573hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602708
Samples
Known GenesAACS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080999
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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