A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190591



Internal ID22341435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36662441..36662493hg38UCSC Ensembl
chr15:36954642..36954694hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456275, nssv14404590, nssv14430248
SamplesNA19240, HG00733, HG00514
Known GenesC15orf41
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190591
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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