A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210232



Internal ID22358186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189501128..189501196hg38UCSC Ensembl
chr3:189218917..189218985hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6305n152
Supporting Variantsnssv14311007, nssv14311008
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210232
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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