A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511273



Internal ID15850698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151331490..151332697hg38UCSC Ensembl
Outerchr4:151314609..151335630hg38UCSC Ensembl
Innerchr4:152252642..152253849hg19UCSC Ensembl
Outerchr4:152235761..152256782hg19UCSC Ensembl
Innerchr4:152472092..152473299hg18UCSC Ensembl
Outerchr4:152455211..152476232hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3821022
hg1921022
hg1821022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624933
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)nsv511273
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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