A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108715



Internal ID22017948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49568414..49568414hg38UCSC Ensembl
chr20:48184951..48184951hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108715
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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