A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217298



Internal ID22363002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124225061..124238520hg38UCSC Ensembl
chr11:124095766..124109221hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3813460
hg1913456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14361475
SamplesHG00513
Known GenesOR8G2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217298
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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