A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208589



Internal ID22356806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66102259..66114360hg38UCSC Ensembl
chr15:66394597..66406698hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3812102
hg1912102
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2959n152
Supporting Variantsnssv14418264
SamplesHG00514
Known GenesMEGF11
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208589
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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