A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996240



Internal ID20563280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10900423..10918106hg38UCSC Ensembl
chr12:11053022..11070705hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3817684
hg1917684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465821
Supporting Variants
Samples
Known GenesPRH1-PRR4, TAS2R13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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