A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3247732



Internal ID22376785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:87145819..87165370hg38UCSC Ensembl
Outerchr15:87689050..87708601hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3817995
hg1917995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258863, nssv14258864
SamplesNA19238, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3247732
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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