A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512239



Internal ID15851664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:95436160..95442545hg38UCSC Ensembl
Outerchr11:95169324..95175709hg19UCSC Ensembl
Outerchr11:94808972..94815357hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386386
hg196386
hg186386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624811
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512239
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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