A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3232492



Internal ID22372517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:84635872..84637381hg38UCSC Ensembl
Outerchr15:85179103..85180612hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14259118
SamplesHG00731
Known GenesSCAND2P
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3232492
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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