A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201063



Internal ID22350421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:111893318..111908692hg38UCSC Ensembl
Outerchr6:112214521..112229895hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3815375
hg1915375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14275595
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201063
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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