A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999972



Internal ID20567012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20854709..21259308hg38UCSC Ensembl
chr12:21007643..21412242hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38404600
hg19404600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463152
Supporting Variants
Samples
Known GenesSLCO1B1, SLCO1B3, SLCO1B7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00038


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