A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106232



Internal ID22015465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39109684..39109684hg38UCSC Ensembl
chr20:37738327..37738327hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106232
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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