A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589146



Internal ID16376555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48061323..48085648hg38UCSC Ensembl
Innerchr22:48457140..48481465hg19UCSC Ensembl
Innerchr22:46835804..46860129hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3824326
hg1924326
hg1824326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957228
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589146
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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