A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554883



Internal ID15995606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55629099hg38UCSC Ensembl
Innerchr11:55371021..55396575hg19UCSC Ensembl
Innerchr11:55127597..55153151hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3825555
hg1925555
hg1825555
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1919n54
Supporting Variantsnssv775967, nssv775969, nssv775968
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554883
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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