A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206157



Internal ID22354741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184593351..184596400hg38UCSC Ensembl
chr3:184311139..184314188hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg383050
hg193050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310870, nssv14310874, nssv14310869, nssv14310875, nssv14310873, nssv14310867, nssv14310868, nssv14310872, nssv14310871
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206157
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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