A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057911



Internal ID18800442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20044066..20069620hg38UCSC Ensembl
Innerchr22:20031589..20057143hg19UCSC Ensembl
Innerchr22:18411589..18437143hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3825555
hg1925555
hg1825555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4479n100
Supporting Variantsnssv3731859, nssv3587354, nssv3731855, nssv3587353, nssv3731857, nssv3731860, nssv3731858, nssv3587357, nssv3587355, nssv3587356, nssv3731856
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)nsv1057911
Frequency
Sample Size29084
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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