A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513747



Internal ID15506482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132054369..132060152hg38UCSC Ensembl
Outerchr11:131924263..131930046hg19UCSC Ensembl
Outerchr11:131429473..131435256hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg385784
hg195784
hg185784
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626999
Samples1
Known GenesNTM
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513747
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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