A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv896797



Internal ID6303808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2177369..2186335hg19UCSC Ensembl
Outerchr11:2176852..2189718hg19UCSC Ensembl
Innerchr11:2133945..2142911hg18UCSC Ensembl
Outerchr11:2133428..2146294hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1499772
SamplesSP50159
Known GenesINS, INS-IGF2, TH
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv896797
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