A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553069



Internal ID15993792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2146073..2162736hg38UCSC Ensembl
Innerchr11:2167303..2183966hg19UCSC Ensembl
Innerchr11:2123879..2140542hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3816664
hg1916664
hg1816664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764482
Samples
Known GenesIGF2, IGF2-AS, INS, INS-IGF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553069
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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