A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367499



Internal ID22593168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111766393..111766393hg38UCSC Ensembl
chr11:111637117..111637117hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974588
Supporting Variants
Samples
Known GenesPPP2R1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367499
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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