A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457484



Internal ID21115037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11013836..11069126hg38UCSC Ensembl
chr12:11166435..11221725hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3855291
hg1955291
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1402n223
Supporting Variantsnssv18183536
Samples
Known GenesPRH1-PRR4, TAS2R19, TAS2R31, TAS2R46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457484
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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