A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2858n152



Internal ID22818561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26194775..26194826hg38UCSC Ensembl
chr15:26439922..26439973hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3212662, nsv3527324
SamplesNA19239, HG00513, HG00514
Known Genes
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)dgv2858n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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