A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109653



Internal ID22018886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5491235..5491235hg38UCSC Ensembl
chr20:5471881..5471881hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109653
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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