A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094045



Internal ID22003278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124296788..124296788hg38UCSC Ensembl
chr11:124166684..124166684hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094045
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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