A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3242896



Internal ID22375415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:41731290..41761896hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282994
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3242896
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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