A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953061



Internal ID16955248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:24410533..24427132hg38UCSC Ensembl
Outerchr22:24806501..24823100hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3816600
hg1916600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000783
SamplesBILGI_BIOE
Known GenesADORA2A, SPECC1L, SPECC1L-ADORA2A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953061
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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