A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511563



Internal ID15504302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907804..89908560hg38UCSC Ensembl
Outerchr16:89904112..89909088hg38UCSC Ensembl
Innerchr16:89974212..89974968hg19UCSC Ensembl
Outerchr16:89970520..89975496hg19UCSC Ensembl
Innerchr16:88501713..88502469hg18UCSC Ensembl
Outerchr16:88498021..88502997hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg384977
hg194977
hg184977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626189
Samples1
Known GenesTCF25
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511563
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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