A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186226



Internal ID22339086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28845771..28845959hg38UCSC Ensembl
chr3:28887262..28887450hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14451079
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)nsv3186226
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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