A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv288n152



Internal ID22815991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79317508..79317598hg38UCSC Ensembl
chr1:79783193..79783283hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3195483, nsv3205667
SamplesNA19238, NA19239, NA19240
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)dgv288n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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