A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14382559



Internal ID22315806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25536304..25536491hg38UCSC Ensembl
chr8:25393820..25394007hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3187425
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14382559
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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