A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100370



Internal ID22009603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:129087941..129087941hg38UCSC Ensembl
chr12:129572486..129572486hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616935
Samples
Known GenesTMEM132D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100370
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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