A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512235



Internal ID15851660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:83126266..83135226hg38UCSC Ensembl
Outerchr11:82837308..82846268hg19UCSC Ensembl
Outerchr11:82514956..82523916hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388961
hg198961
hg188961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624806
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)nsv512235
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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