A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554890



Internal ID15995613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55650706hg38UCSC Ensembl
Innerchr11:55371021..55418182hg19UCSC Ensembl
Innerchr11:55127597..55174758hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3847162
hg1947162
hg1847162
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1913n54
Supporting Variantsnssv775993, nssv775994, nssv775991, nssv775992, nssv775995
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554890
Frequency
Sample Size17421
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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