A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459258



Internal ID21116811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:86286901..86311100hg38UCSC Ensembl
chr12:86680679..86704878hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3824200
hg1924200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188022
Samples
Known GenesMGAT4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459258
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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