A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513686



Internal ID15853107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:74281858..74283397hg38UCSC Ensembl
Outerchr9:76896774..76898313hg19UCSC Ensembl
Outerchr9:76086594..76088133hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381540
hg191540
hg181540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626938
Samples1
Known GenesMIR6130
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513686
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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