A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2921n152



Internal ID22818624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49489788..49489848hg38UCSC Ensembl
chr15:49781985..49782045hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3283816, nsv3287612
SamplesNA19240, HG00733, HG00514
Known GenesFAM227B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2921n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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