A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025286



Internal ID21934629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111933541..111933636hg38UCSC Ensembl
chr12:112371345..112371440hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617261
Samples
Known GenesTMEM116
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025286
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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