A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189628



Internal ID22340874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72447090..72447581hg38UCSC Ensembl
chr3:72496241..72496732hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6010n152
Supporting Variantsnssv14450487
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)nsv3189628
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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