A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181392



Internal ID22336549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98915524..98915627hg38UCSC Ensembl
chr3:98634368..98634471hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14409393
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)nsv3181392
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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