A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196787



Internal ID22346744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:158921090..158934020hg38UCSC Ensembl
Outerchr6:159342122..159355052hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3812931
hg1912931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277292
SamplesHG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196787
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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