A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6738690



Internal ID9801616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:23931964..23969096hg38UCSC Ensembl
Outerchr22:24274151..24311285hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3837133
hg1937135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2724041, esv2724066
Supporting Variants
SamplesSSM050
Known GenesDDTL, GSTT2, GSTT2B
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6738690
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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