A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670432



Internal ID21618737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17659212..17659212hg38UCSC Ensembl
chr20:17639857..17639857hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116451
SamplesHG00731
Known GenesRRBP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670432
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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