A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066874



Internal ID18809405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38903097..38955461hg38UCSC Ensembl
Innerchr22:39299102..39351466hg19UCSC Ensembl
Innerchr22:37629048..37681412hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3852365
hg1952365
hg1852365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600888
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)nsv1066874
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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