A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv951976



Internal ID15899246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21953009..22219245hg38UCSC Ensembl
Innerchr22:22307381..22573637hg19UCSC Ensembl
Innerchr22:20637381..20903637hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38266237
hg19266257
hg18266257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588325
Supporting Variants
Samples
Known GenesTOP3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv951976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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