A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv954559



Internal ID15901829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:30265195..30295642hg38UCSC Ensembl
Innerchr22:30661184..30691631hg19UCSC Ensembl
Innerchr22:28991184..29021631hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3830448
hg1930448
hg1830448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588885
Supporting Variants
Samples
Known GenesGATSL3, OSM, TBC1D10A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv954559
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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