A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228201



Internal ID22370464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41380094..41465621hg38UCSC Ensembl
Outerchr15:41672292..41757819hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3885528
hg1985528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258471
SamplesHG00513
Known GenesNDUFAF1, NUSAP1, RTF1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228201
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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