A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512198



Internal ID15504937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:676286..678291hg38UCSC Ensembl
Outerchr11:676286..678291hg19UCSC Ensembl
Outerchr11:666286..668291hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382006
hg192006
hg182006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624765
Samples1
Known GenesDEAF1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512198
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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