A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513652



Internal ID15853073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:128628295..128659576hg38UCSC Ensembl
Outerchr3:128347138..128378419hg19UCSC Ensembl
Outerchr3:129829828..129861109hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3831282
hg1931282
hg1831282
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv36n50
Supporting Variantsnssv626904
Samples1
Known GenesRPN1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513652
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer