A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996256



Internal ID20563296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10925220..10950133hg38UCSC Ensembl
chr12:11077819..11102732hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3824914
hg1924914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456082
Supporting Variants
Samples
Known GenesPRH1-PRR4, PRH2, TAS2R14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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