A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14463485



Internal ID22215992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26277097..26277459hg38UCSC Ensembl
chr8:26134613..26134975hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3176657
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)nssv14463485
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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