A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8664n152



Internal ID22824367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98751851..98755150hg38UCSC Ensembl
chr7:98381163..98384483hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383300
hg193321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3198273, nsv3207603
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)dgv8664n152
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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