A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4906n71



Internal ID6322526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24000993..24368161hg19UCSC Ensembl
chr22:22330993..22698161hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv914594, nsv914596
SamplesSP80994, MS15458
Known GenesC22orf15, CHCHD10, DDT, DDTL, DERL3, GSTT2, GSTT2B, GSTTP1, GUSBP11, LOC284889, MIF, MMP11, RGL4, SLC2A11, SMARCB1, VPREB3, ZNF70
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv4906n71
Frequency
Sample Size6533
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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