A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089263



Internal ID21998496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68929877..68929877hg38UCSC Ensembl
chr11:68697345..68697345hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587705
Samples
Known GenesIGHMBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089263
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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