A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093789



Internal ID22003022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62143024..62143024hg38UCSC Ensembl
chr11:61910496..61910496hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578851
Samples
Known GenesINCENP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093789
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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