A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8666n152



Internal ID22824369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99212701..99223950hg38UCSC Ensembl
chr7:98810324..98821573hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3811250
hg1911250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3199477, nsv3200785
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, 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)dgv8666n152
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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