A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553133



Internal ID16340542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3247045..3338059hg38UCSC Ensembl
Innerchr11:3268275..3359289hg19UCSC Ensembl
Innerchr11:3224851..3315865hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3891015
hg1991015
hg1891015
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1577n54
Supporting Variantsnssv764595, nssv764592, nssv764593, nssv764588, nssv764594, nssv764591, nssv764590, nssv764589, nssv764587, nssv764596
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553133
Frequency
Sample Size17421
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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