A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199353



Internal ID22348948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144686186..144688927hg38UCSC Ensembl
chr8:145911571..145914312hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg382742
hg192742
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439797, nssv14439798
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199353
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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