A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv896793



Internal ID6303804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2176042..2179313hg19UCSC Ensembl
Outerchr11:2174887..2181073hg19UCSC Ensembl
Innerchr11:2132618..2135889hg18UCSC Ensembl
Outerchr11:2131463..2137649hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1506996
SamplesSP54448
Known GenesINS, INS-IGF2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv896793
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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