A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101680



Internal ID22010845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2483383..2483383hg38UCSC Ensembl
chr20:2464029..2464029hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637003
Samples
Known GenesZNF343
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101680
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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