A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589174



Internal ID16376583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48998499..49462025hg38UCSC Ensembl
Innerchr22:49394311..49855674hg19UCSC Ensembl
Innerchr22:47780315..48241678hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg38463527
hg19461364
hg18461364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8132n54
Supporting Variantsnssv957300
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589174
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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