A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995693



Internal ID20562733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104266615..104266746hg38UCSC Ensembl
chr12:104660393..104660524hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466854
Supporting Variants
Samples
Known GenesTXNRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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