A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779159



Internal ID18821335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23947178..24001082hg38UCSC Ensembl
Innerchr22:24289365..24346385hg19UCSC Ensembl
Innerchr22:22619365..22676385hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3853905
hg1957021
hg1857021
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893452
Supporting Variants
Samples
Known GenesDDT, DDTL, GSTT2, GSTT2B, GSTTP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779159
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer