A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv896005



Internal ID6303016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112836193..112844268hg19UCSC Ensembl
Outerchr10:112835992..112846298hg19UCSC Ensembl
Innerchr10:112826183..112834258hg18UCSC Ensembl
Outerchr10:112825982..112836288hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510520
SamplesSP54967
Known GenesADRA2A
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv896005
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer