A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511209



Internal ID15850634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116951543..117077269hg38UCSC Ensembl
Outerchr3:116950316..117080547hg38UCSC Ensembl
Innerchr3:116670390..116796116hg19UCSC Ensembl
Outerchr3:116669163..116799394hg19UCSC Ensembl
Innerchr3:118153080..118278806hg18UCSC Ensembl
Outerchr3:118151853..118282084hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38130232
hg19130232
hg18130232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626654
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511209
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