A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459606



Internal ID21117159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:86575701..86630000hg38UCSC Ensembl
chr12:86969478..87023777hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg3854300
hg1954300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196813
Samples
Known GenesMGAT4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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