A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614453



Internal ID21806500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:129087944..129087944hg38UCSC Ensembl
chr12:129572489..129572489hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082922
Supporting Variants
Samples
Known GenesTMEM132D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614453
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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