A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208476



Internal ID22356711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:141709797..141742355hg38UCSC Ensembl
Outerchr6:142030934..142063492hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3832559
hg1932559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14275988
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208476
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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