A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559095



Internal ID22427898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102471142..102471142hg38UCSC Ensembl
chr11:102341873..102341873hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359899, nssv14359898, nssv14359900
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559095
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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