A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357293



Internal ID22210474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3096908..3097124hg38UCSC Ensembl
chr11:3118138..3118354hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528600
Supporting Variants
SamplesHG00732
Known GenesOSBPL5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357293
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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