A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8732n152



Internal ID22824435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122705693..122705969hg38UCSC Ensembl
chr7:122345747..122346023hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3288293, nsv3527847
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesCADPS2
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)dgv8732n152
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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