A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099239



Internal ID22008472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109868067..109868067hg38UCSC Ensembl
chr12:110305872..110305872hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615609
Samples
Known GenesGLTP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099239
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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