A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083443



Internal ID21992676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92214294..92214294hg38UCSC Ensembl
chr11:91947460..91947460hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083443
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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