A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181649



Internal ID22336684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20301220..20301401hg38UCSC Ensembl
chr3:20342712..20342893hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5895n152
Supporting Variantsnssv14451045
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)nsv3181649
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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