A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191790



Internal ID22342450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171006248..171006308hg38UCSC Ensembl
chr3:170724037..170724097hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310597
SamplesNA19238
Known GenesSLC2A2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191790
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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