A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186013



Internal ID22338969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184752139..184755856hg38UCSC Ensembl
chr3:184469927..184473644hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg383718
hg193718
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6289n152
Supporting Variantsnssv14435350, nssv14435351
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3186013
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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