A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101455



Internal ID22010688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19050444..19050444hg38UCSC Ensembl
chr20:19031088..19031088hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101455
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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