A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526384



Internal ID22395765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3116966..3117035hg38UCSC Ensembl
chr3:3158650..3158719hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5844n152
Supporting Variantsnssv14303734, nssv14303738, nssv14303735, nssv14303737, nssv14303736
SamplesHG00512, NA19239, HG00731, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526384
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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