A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14420898



Internal ID22158722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8621707..8629080hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387374
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207536
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14420898
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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