A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626937



Internal ID15850469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:117995786..118003221hg38UCSC Ensembl
Outerchr8:119008025..119015460hg19UCSC Ensembl
Outerchr8:119077206..119084641hg18UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg387436
hg197436
hg187436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513685
Supporting Variants
Samples1
Known GenesEXT1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626937
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