A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3368n152



Internal ID22819071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:136265..136358hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3285468, nsv3288822
SamplesNA19240, HG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv3368n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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