A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193627



Internal ID22344056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5079317..5079667hg38UCSC Ensembl
chr3:5121002..5121352hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14303800, nssv14303801
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193627
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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