A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554882



Internal ID15995605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55628565hg38UCSC Ensembl
Innerchr11:55371021..55396041hg19UCSC Ensembl
Innerchr11:55127597..55152617hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3825021
hg1925021
hg1825021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1918n54
Supporting Variantsnssv775965, nssv775966
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554882
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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