A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067456



Internal ID19156675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:34662127..34696482hg38UCSC Ensembl
Innerchr22:35058119..35092473hg19UCSC Ensembl
Innerchr22:33388119..33422473hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3834356
hg1934355
hg1834355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600840
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067456
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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