A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109190



Internal ID22018423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9603210..9603210hg38UCSC Ensembl
chr18:9603208..9603208hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg383012
hg193012
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629455
Samples
Known GenesPPP4R1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109190
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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