A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2855n152



Internal ID22818558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25966883..25966998hg38UCSC Ensembl
chr15:26212030..26212145hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3287327, nsv3219653
SamplesNA19238, HG00731, NA19240, HG00513
Known GenesLOC100128714
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2855n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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