A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv890854



Internal ID6297865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:49745347..49830142hg19UCSC Ensembl
Outerchr8:49738821..49838908hg19UCSC Ensembl
Innerchr8:49907900..49992695hg18UCSC Ensembl
Outerchr8:49901374..50001461hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1572352
SamplesIS32998
Known GenesSNAI2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv890854
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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