A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589178



Internal ID16376587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:49077935..49584927hg38UCSC Ensembl
Innerchr22:49473747..49978575hg19UCSC Ensembl
Innerchr22:47859751..48364579hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg38506993
hg19504829
hg18504829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8132n54
Supporting Variantsnssv957304
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589178
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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