A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv949490



Internal ID16243446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16376478..16390411hg38UCSC Ensembl
Innerchr22:16857140..16871137hg19UCSC Ensembl
Innerchr22:15237140..15251137hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3813934
hg1913998
hg1813998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588058
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv949490
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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