A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198109



Internal ID22347884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81323240..81323318hg38UCSC Ensembl
chr15:81615581..81615659hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14405374
SamplesNA19240
Known GenesSTARD5
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198109
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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