A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083423



Internal ID21992656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64213420..64213420hg38UCSC Ensembl
chr11:63980892..63980892hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579565
Samples
Known GenesFERMT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083423
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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