A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752056



Internal ID20527916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44764022..44764022hg38UCSC Ensembl
chr20:43392663..43392663hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260133
Samples
Known GenesRIMS4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752056
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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