A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14417697



Internal ID22154039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90871538..90871885hg38UCSC Ensembl
chr15:91414768..91415115hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3193487
Supporting Variants
SamplesHG00514
Known GenesFURIN
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14417697
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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