A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3283074



Internal ID22381413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114241706..114241790hg38UCSC Ensembl
chr5:113577403..113577487hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7485n152
Supporting Variantsnssv14410598
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3283074
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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