A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626963



Internal ID15503809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:12809752..12812518hg38UCSC Ensembl
Outerchr19:12920566..12923332hg19UCSC Ensembl
Outerchr19:12781566..12784332hg18UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg382767
hg192767
hg182767
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513711
Supporting Variants
Samples1
Known GenesRNASEH2A
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626963
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