A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3238945



Internal ID22374295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:83225654..83247745hg38UCSC Ensembl
Outerchr15:83894406..83916497hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg383963
hg193963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14259660, nssv14259662, nssv14259661
SamplesNA19238, NA19240, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3238945
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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