A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv955459



Internal ID16249415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35545973..35582568hg38UCSC Ensembl
Innerchr22:35942020..35978615hg19UCSC Ensembl
Innerchr22:34271966..34308561hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3836596
hg1936596
hg1836596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588949
Supporting Variants
Samples
Known GenesRASD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv955459
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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