A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv159n152



Internal ID22815862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28880308..28880677hg38UCSC Ensembl
chr1:29206820..29207189hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3196943, nsv3196831
SamplesHG00512, NA19238, HG00731, NA19240, HG00733, 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)dgv159n152
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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