A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3003n152



Internal ID22818706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79840176..79840239hg38UCSC Ensembl
chr15:80132518..80132581hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3286859, nsv3529121
SamplesNA19238, NA19239, 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)dgv3003n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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