A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3244277



Internal ID22375819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103197238..103208570hg38UCSC Ensembl
Outerchr10:104956995..104968327hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg388801
hg198801
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252904, nssv14252903
SamplesHG00732, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3244277
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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