A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512102



Internal ID15504841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69123086..69128466hg38UCSC Ensembl
Outerchr9:71738002..71743382hg19UCSC Ensembl
Outerchr9:70927822..70933202hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385381
hg195381
hg185381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624659
Samples1
Known GenesTJP2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512102
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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