A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186007



Internal ID20753047
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 StatusS
Merged Variantsnsv6465372
Supporting Variants
Samples
Known GenesPRH1, PRH1-PRR4, PRR4, TAS2R10, TAS2R7, TAS2R8, TAS2R9, YBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186007
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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