A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109553



Internal ID22018786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3788752..3788752hg38UCSC Ensembl
chr20:3769399..3769399hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109553
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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