A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625729



Internal ID15849262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:121329221..121329634hg38UCSC Ensembl
Outerchr11:121199930..121200343hg19UCSC Ensembl
Outerchr11:120705140..120705553hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381134
hg191134
hg181134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513338
Supporting Variants
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)nssv625729
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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