A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193288



Internal ID22343751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181856993..181857397hg38UCSC Ensembl
chr3:181574781..181575185hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310138, nssv14310136, nssv14310135, nssv14310137
SamplesNA19239, HG00731, HG00732, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193288
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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