A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559690



Internal ID22428490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60525910..60525910hg38UCSC Ensembl
chr11:60293383..60293383hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359626, nssv14359625
SamplesNA19239, NA19240
Known GenesMS4A13
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559690
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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