A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3239822



Internal ID22374542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:102737417..102740384hg38UCSC Ensembl
Outerchr14:103203754..103206721hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg384163
hg194163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258232
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3239822
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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