A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067162



Internal ID18809693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25738059..25751045hg38UCSC Ensembl
Innerchr22:26134026..26147012hg19UCSC Ensembl
Innerchr22:24464026..24477012hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3812987
hg1912987
hg1812987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600785
Samples
Known GenesMYO18B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067162
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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