A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14377631



Internal ID22324172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66102259..66114389hg38UCSC Ensembl
chr15:66394597..66406727hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3812131
hg1912131
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201500
Supporting Variants
SamplesNA19240
Known GenesMEGF11
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14377631
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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