A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553157



Internal ID16340566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4366530..4392730hg38UCSC Ensembl
Innerchr11:4387760..4413960hg19UCSC Ensembl
Innerchr11:4344336..4370536hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826201
hg1926201
hg1826201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1582n54
Supporting Variantsnssv764646
Samples
Known GenesOR52B4, TRIM21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553157
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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