A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467720



Internal ID21125273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11028946..11090022hg38UCSC Ensembl
chr12:11181545..11242621hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3861077
hg1961077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1403n223
Supporting Variantsnssv18187686
Samples
Known GenesPRH1-PRR4, TAS2R31, TAS2R46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467720
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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