A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060198



Internal ID19149417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:34686377..34745602hg38UCSC Ensembl
Innerchr22:35082368..35141593hg19UCSC Ensembl
Innerchr22:33412368..33471593hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3859226
hg1959226
hg1859226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600841
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)nsv1060198
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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