A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205863



Internal ID22354490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42471069..42471127hg38UCSC Ensembl
chr3:42512561..42512619hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5949n152
Supporting Variantsnssv14306120, nssv14306121
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205863
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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