A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193841



Internal ID22344237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143031398..143031471hg38UCSC Ensembl
chr3:142750240..142750313hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14309614, nssv14309613
SamplesNA19238, NA19240
Known GenesU2SURP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193841
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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