A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108471



Internal ID22017705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52770904..52770904hg38UCSC Ensembl
chr20:51387443..51387443hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108471
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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