A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227353



Internal ID22369875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:96454266..96471377hg38UCSC Ensembl
Outerchr15:96997496..97014607hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3817112
hg1917112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258840, nssv14258842, nssv14258841
SamplesNA19238, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227353
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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