A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193487



Internal ID22343927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90871538..90871885hg38UCSC Ensembl
chr15:91414768..91415115hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14445777, nssv14373430, nssv14417697
SamplesNA19240, HG00733, HG00514
Known GenesFURIN
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193487
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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