A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099229



Internal ID22008462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62426177..62426177hg38UCSC Ensembl
chr11:62193649..62193649hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099229
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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