A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101793



Internal ID22011026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34286388..34286388hg38UCSC Ensembl
chr20:32874194..32874194hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623628
Samples
Known GenesAHCY
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101793
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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