A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021212



Internal ID21930555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108907211..108907264hg38UCSC Ensembl
chr12:109300987..109301040hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021212
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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