A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178200



Internal ID22334856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20301220..20301402hg38UCSC Ensembl
chr3:20342712..20342894hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5895n152
Supporting Variantsnssv14396526
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)nsv3178200
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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