A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14409369



Internal ID22287993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86767546..86767607hg38UCSC Ensembl
chr3:86816696..86816757hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179062
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)nssv14409369
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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