A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14466096



Internal ID22218373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94546051..94546105hg38UCSC Ensembl
chr15:95089280..95089334hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206499
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14466096
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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