A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110029



Internal ID22019262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46543305..46543305hg38UCSC Ensembl
chr20:45171944..45171944hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635493
Samples
Known GenesOCSTAMP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110029
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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