A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2966013



Internal ID10638993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23957813..23991806hg38UCSC Ensembl
Innerchr22:24300000..24334000hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3833994
hg1934001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7235580
SamplesHuRef
Known GenesDDT, DDTL, GSTT2, GSTT2B
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2966013
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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