A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552777



Internal ID15993500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:368778..382912hg38UCSC Ensembl
Innerchr11:368778..382912hg19UCSC Ensembl
Innerchr11:358778..372912hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3814135
hg1914135
hg1814135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1507n54
Supporting Variantsnssv763061
Samples
Known GenesB4GALNT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552777
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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