A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512213



Internal ID15851638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:24327091..24334557hg38UCSC Ensembl
Outerchr11:24348637..24356103hg19UCSC Ensembl
Outerchr11:24305213..24312679hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg387467
hg197467
hg187467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624782
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)nsv512213
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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