A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14418264



Internal ID22154856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66102259..66114360hg38UCSC Ensembl
chr15:66394597..66406698hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3812102
hg1912102
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208589
Supporting Variants
SamplesHG00514
Known GenesMEGF11
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14418264
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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