A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152115



Internal ID15853774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22438063..22488632hg38UCSC Ensembl
Innerchr22:22792400..22842957hg19UCSC Ensembl
Innerchr22:21122400..21172957hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg3850570
hg1950558
hg1850558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588461
Supporting Variants
Samples1780854436_A
Known GenesZNF280B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152115
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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