A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215201



Internal ID22361612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:36047733..36099060hg38UCSC Ensembl
Outerchr15:36339934..36391261hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3851328
hg1951328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258470
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215201
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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