A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv954553



Internal ID16248509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:27534119..27698847hg38UCSC Ensembl
Innerchr22:27930080..28094845hg19UCSC Ensembl
Innerchr22:26260080..26424845hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38164729
hg19164766
hg18164766
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588877
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv954553
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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