A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764888



Internal ID20540748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109868105..109868105hg38UCSC Ensembl
chr12:110305910..110305910hg19UCSC 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 Variantsnssv16296421
Samples
Known GenesGLTP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764888
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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