A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106530



Internal ID22015763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17659571..17659571hg38UCSC Ensembl
chr20:17640216..17640216hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632006
Samples
Known GenesRRBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106530
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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