A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553349



Internal ID16340758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5878655..5933579hg38UCSC Ensembl
Innerchr11:5899885..5954809hg19UCSC Ensembl
Innerchr11:5856461..5911385hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3854925
hg1954925
hg1854925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1623n54
Supporting Variantsnssv1174607, nssv1174608
SamplesHGDP01194, HGDP01321
Known GenesOR52E4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553349
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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