A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996110



Internal ID20563150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106372407..106374584hg38UCSC Ensembl
chr12:106766185..106768362hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382178
hg192178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467731
Supporting Variants
Samples
Known GenesPOLR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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