A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553590



Internal ID16340999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17875867..17889117hg38UCSC Ensembl
Innerchr11:17897414..17910664hg19UCSC Ensembl
Innerchr11:17853990..17867240hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3813251
hg1913251
hg1813251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768331
Samples
Known GenesSERGEF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553590
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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