A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208434



Internal ID22356677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25054266..25058521hg38UCSC Ensembl
chr3:25095757..25100012hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg384256
hg194256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14306494, nssv14306493, nssv14306492
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208434
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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