A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3249615



Internal ID22377326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:45050864..45055553hg38UCSC Ensembl
Outerchr21:46470779..46475468hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14267716, nssv14268773, nssv14267718, nssv14267717, nssv14268774
SamplesNA19239, HG00732, NA19240, HG00733, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3249615
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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