A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4536n100



Internal ID20156152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23940817..24001082hg38UCSC Ensembl
chr22:24283004..24360423hg19UCSC Ensembl
chr22:22613004..22690423hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3860266
hg1977420
hg1877420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061823, nsv1065133, nsv1055299
Samples
Known GenesDDT, DDTL, GSTT2, GSTT2B, GSTTP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4536n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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