A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083791



Internal ID21993024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1486897..1486897hg38UCSC Ensembl
chr11:1508127..1508127hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590119
Samples
Known GenesMOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083791
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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