A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062841



Internal ID18805372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20122027..20291605hg38UCSC Ensembl
Innerchr22:20109550..20279128hg19UCSC Ensembl
Innerchr22:18489550..18659128hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38169579
hg19169579
hg18169579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4481n100
Supporting Variantsnssv3587365
Samples
Known GenesLINC00896, LOC284865, LOC388849, MIR1286, RANBP1, RTN4R, ZDHHC8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062841
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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