A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191766



Internal ID22342431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:141584404..141659931hg38UCSC Ensembl
Outerchr6:141905541..141981068hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3875528
hg1975528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277272
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191766
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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