A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513633



Internal ID15506368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:2553995..2567688hg38UCSC Ensembl
Outerchr1:2485434..2499127hg19UCSC Ensembl
Outerchr1:2473504..2489016hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3813694
hg1913694
hg1815513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1n50
Supporting Variantsnssv626885
Samples1
Known GenesLOC100133445, LOC115110, TNFRSF14
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513633
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