A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106091



Internal ID22015324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37247269..37247269hg38UCSC Ensembl
chr20:35875672..35875672hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106091
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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