A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511473



Internal ID15850898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34182173..34182917hg38UCSC Ensembl
Outerchr11:34181406..34191336hg38UCSC Ensembl
Innerchr11:34203720..34204464hg19UCSC Ensembl
Outerchr11:34202953..34212883hg19UCSC Ensembl
Innerchr11:34160296..34161040hg18UCSC Ensembl
Outerchr11:34159529..34169459hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg389931
hg199931
hg189931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626089
Samples1
Known GenesABTB2
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511473
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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