A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv896776



Internal ID6303787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2117403..2333675hg19UCSC Ensembl
Outerchr11:2108794..2339737hg19UCSC Ensembl
Innerchr11:2073979..2290251hg18UCSC Ensembl
Outerchr11:2065370..2296313hg18UCSC 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 Variantsnssv1543596
SamplesMS16153
Known GenesASCL2, C11orf21, IGF2, IGF2AS, INS, INS-IGF2, MIR4686, MIR483, TH, TSPAN32
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv896776
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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