A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512989



Internal ID15852411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:71281722..71282449hg38UCSC Ensembl
Outerchr9:73896638..73897365hg19UCSC Ensembl
Outerchr9:73086458..73087185hg18UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38836
hg19836
hg18836
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625645
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)nsv512989
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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