A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553175



Internal ID16340584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4769038..4769334hg38UCSC Ensembl
Innerchr11:4790268..4790564hg19UCSC Ensembl
Innerchr11:4746844..4747140hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38297
hg19297
hg18297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764668, nssv764669
Samples
Known GenesOR51F1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553175
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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