A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8566n152



Internal ID22824269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66392627..66395118hg38UCSC Ensembl
chr7:65857614..65860105hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382492
hg192492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3201438, nsv3285701
SamplesHG00512, NA19238, HG00731, HG00732, NA19240, HG00513, HG00514
Known GenesLINC00174
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)dgv8566n152
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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