A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589051



Internal ID16376460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:41731777..41794305hg38UCSC Ensembl
Innerchr22:42127781..42190309hg19UCSC Ensembl
Innerchr22:40457727..40520255hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3862529
hg1962529
hg1862529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8111n54
Supporting Variantsnssv957089
Samples
Known GenesMEI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589051
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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