A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4479n100



Internal ID20156095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20039773..20069620hg38UCSC Ensembl
chr22:20027296..20057143hg19UCSC Ensembl
chr22:18407296..18437143hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3829848
hg1929848
hg1829848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063777, nsv1062524, nsv1057911
Samples
Known GenesTANGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4479n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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