A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106285



Internal ID22015518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22561929..22561929hg38UCSC Ensembl
chr20:22542567..22542567hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619536
Samples
Known GenesLINC00261
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106285
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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