A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655163



Internal ID21603468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3613685..3613685hg38UCSC Ensembl
chr20:3594332..3594332hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116875
SamplesNA19650
Known GenesATRN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655163
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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