A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106655



Internal ID22015889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58948422..58948422hg38UCSC Ensembl
chr20:57523477..57523477hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106655
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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