A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097495



Internal ID22006728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:197206..197206hg38UCSC Ensembl
chr12:306372..306372hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601278
Samples
Known GenesSLC6A12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097495
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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