A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553313



Internal ID16340722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5760659..5781623hg38UCSC Ensembl
Innerchr11:5781889..5802853hg19UCSC Ensembl
Innerchr11:5738465..5759429hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3820965
hg1920965
hg1820965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1617n54
Supporting Variantsnssv765910
Samples
Known GenesOR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553313
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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