A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067233



Internal ID19156452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:41721635..41773265hg38UCSC Ensembl
Innerchr22:42117639..42169269hg19UCSC Ensembl
Innerchr22:40447585..40499215hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3851631
hg1951631
hg1851631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590814
Samples
Known GenesMEI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067233
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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