A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589158



Internal ID16029881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48497621..48499962hg38UCSC Ensembl
Innerchr22:48893433..48895774hg19UCSC Ensembl
Innerchr22:47272097..47274438hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg382342
hg192342
hg182342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8128n54
Supporting Variantsnssv957273, nssv957274
Samples
Known GenesFAM19A5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589158
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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