A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5697n152



Internal ID22821400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24605966..24606041hg38UCSC Ensembl
chr22:25001933..25002008hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3210985, nsv3297829
SamplesHG00512, HG00732, HG00733, HG00514
Known GenesGGT1
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)dgv5697n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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