A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186632



Internal ID22339304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129356011..129364611hg38UCSC Ensembl
chr3:129074854..129083454hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg388601
hg198601
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14410241
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3186632
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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