A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190490



Internal ID22341346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77117793..77118071hg38UCSC Ensembl
chr15:77410135..77410413hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14418131
SamplesHG00514
Known GenesPEAK1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190490
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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