A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055299



Internal ID18797830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23943610..24001082hg38UCSC Ensembl
Innerchr22:24285797..24360423hg19UCSC Ensembl
Innerchr22:22615797..22690423hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3857473
hg1974627
hg1874627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4536n100
Supporting Variantsnssv3586680
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)nsv1055299
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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