A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097979



Internal ID22007212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3429086..3429086hg38UCSC Ensembl
chr12:3538252..3538252hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604691
Samples
Known GenesPRMT8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097979
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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