A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187599



Internal ID22339812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38326853..38326920hg38UCSC Ensembl
chr3:38368344..38368411hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14435260
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3187599
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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