A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465372



Internal ID21122925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10720422..10881002hg38UCSC Ensembl
chr12:10873021..11033601hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38160581
hg19160581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186007
Samples
Known GenesPRH1, PRH1-PRR4, PRR4, TAS2R10, TAS2R7, TAS2R8, TAS2R9, YBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465372
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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