A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171434



Internal ID22331293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19479764..19479834hg38UCSC Ensembl
chr8:19337275..19337345hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9094n152
Supporting Variantsnssv14455632
SamplesHG00733
Known GenesCSGALNACT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3171434
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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