A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640911



Internal ID21832958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50344810..50344810hg38UCSC Ensembl
chr22:50783239..50783239hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101351
Supporting Variants
Samples
Known GenesPPP6R2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640911
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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