A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553350



Internal ID16340759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5878655..5938527hg38UCSC Ensembl
Innerchr11:5899885..5959757hg19UCSC Ensembl
Innerchr11:5856461..5916333hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3859873
hg1959873
hg1859873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1623n54
Supporting Variantsnssv1174609, nssv1174611, nssv1174610
SamplesHGDP00968, HGDP01097, HGDP01322
Known GenesOR52E4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553350
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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