A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228136



Internal ID22370414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:114343367..114449237hg38UCSC Ensembl
Outerchr8:115355596..115461466hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38105871
hg19105871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14278878
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228136
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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