A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3245394



Internal ID22376133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:3077220..3091053hg38UCSC Ensembl
Outerchr19:3077218..3091051hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14263798
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3245394
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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