A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14425197



Internal ID22164970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188951846..188952184hg38UCSC Ensembl
chr3:188669635..188669973hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3183091
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)nssv14425197
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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