A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14397787



Internal ID22318223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183685076..183686616hg38UCSC Ensembl
chr3:183402864..183404404hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381541
hg191541
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3181670
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)nssv14397787
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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