A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv830e199



Internal ID22758603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37946213..37948626hg38UCSC Ensembl
chr22:38342220..38344633hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382414
hg192414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658288, esv2667264
SamplesNA19462, NA19257
Known GenesC22orf23
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv830e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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