A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8369n152



Internal ID22824072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2859405..2859563hg38UCSC Ensembl
chr7:2899039..2899197hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3288685, nsv3528140
SamplesHG00732, 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)dgv8369n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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