A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511455



Internal ID15850880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18552866..18564652hg38UCSC Ensembl
Outerchr10:18548356..18565239hg38UCSC Ensembl
Innerchr10:18841795..18853581hg19UCSC Ensembl
Outerchr10:18837285..18854168hg19UCSC Ensembl
Innerchr10:18881801..18893587hg18UCSC Ensembl
Outerchr10:18877291..18894174hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3816884
hg1916884
hg1816884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626069
Samples1
Known GenesNSUN6
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511455
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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