A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3243698



Internal ID22375649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:61461679..61481134hg38UCSC Ensembl
Outerchr15:61753878..61773333hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg385885
hg195885
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14259579
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3243698
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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