A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101586



Internal ID22010819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33057478..33057478hg38UCSC Ensembl
chr20:31645284..31645284hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618583
Samples
Known GenesBPIFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101586
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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