A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3241862



Internal ID22375090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131397996..131420134hg38UCSC Ensembl
Outerchr10:133196259..133218397hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253769
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3241862
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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