A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466215



Internal ID21123768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25106344..25114717hg38UCSC Ensembl
chr12:25259278..25267651hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg388374
hg198374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188968
Samples
Known GenesCASC1, LRMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466215
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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