A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229327



Internal ID22371211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2862684..2863031hg38UCSC Ensembl
chr16:2912685..2913032hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3115n152
Supporting Variantsnssv14403668
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229327
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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