A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3587360



Internal ID18538955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20080968..20262667hg38UCSC Ensembl
Innerchr22:20068491..20250190hg19UCSC Ensembl
Innerchr22:18448491..18630190hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38181700
hg19181700
hg18181700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058048
Supporting Variants
Samples
Known GenesDGCR8, LINC00896, LOC284865, LOC388849, MIR1286, MIR1306, MIR3618, MIR6816, RANBP1, RTN4R, TRMT2A, ZDHHC8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3587360
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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