A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022734



Internal ID21932077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54185467..54185526hg38UCSC Ensembl
chr12:54579251..54579310hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604162
Samples
Known GenesSMUG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022734
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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