A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089682



Internal ID21998915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63618434..63618434hg38UCSC Ensembl
chr11:63385906..63385906hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089682
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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