A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513710



Internal ID15853131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:43323793..43389405hg38UCSC Ensembl
Outerchr17:41401161..41466773hg19UCSC Ensembl
Outerchr17:38756687..38822299hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3865613
hg1965613
hg1865613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626962
Samples1
Known GenesLINC00910
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513710
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