A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511458



Internal ID15850883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87516131..87516650hg38UCSC Ensembl
Outerchr10:87513822..87532880hg38UCSC Ensembl
Innerchr10:89275888..89276407hg19UCSC Ensembl
Outerchr10:89273579..89292637hg19UCSC Ensembl
Innerchr10:89265868..89266387hg18UCSC Ensembl
Outerchr10:89263559..89282617hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3819059
hg1919059
hg1819059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626072
Samples1
Known GenesMINPP1
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511458
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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