A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3282355



Internal ID22380689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150821839..150822040hg38UCSC Ensembl
chr3:150539626..150539827hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14410310
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)nsv3282355
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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