A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3249262



Internal ID22377228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:50777734..50785925hg38UCSC Ensembl
Outerchr19:51280991..51289182hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14263616, nssv14263618, nssv14263617, nssv14263619
SamplesHG00512, NA19239, HG00731, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3249262
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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