A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv825566



Internal ID6138606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112830014..112871333hg19UCSC Ensembl
Innerchr10:112820004..112861323hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1439089
SamplesNA18973
Known GenesADRA2A
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv825566
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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