A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602244



Internal ID21794291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94593470..94593470hg38UCSC Ensembl
chr12:94987246..94987246hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092525
Supporting Variants
Samples
Known GenesTMCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602244
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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