A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553236



Internal ID16340645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5361785..5362477hg38UCSC Ensembl
Innerchr11:5383015..5383707hg19UCSC Ensembl
Innerchr11:5339591..5340283hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38693
hg19693
hg18693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1599n54
Supporting Variantsnssv765360, nssv765361, nssv765362
Samples
Known GenesOR51B5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553236
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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