A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv829155



Internal ID6134245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:29664396..29724001hg19UCSC Ensembl
Innerchr22:27994396..28054001hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1435622
SamplesNA18942
Known GenesAP1B1, EWSR1, GAS2L1, RASL10A
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv829155
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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