A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2856n152



Internal ID22818559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25999825..25999895hg38UCSC Ensembl
chr15:26244972..26245042hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3220554, nsv3214886
SamplesHG00512, NA19240, HG00513, HG00514
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)dgv2856n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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