A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996936



Internal ID20563976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110720868..110721099hg38UCSC Ensembl
chr12:111158673..111158904hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484997
Supporting Variants
Samples
Known GenesPPP1CC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00121


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