A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511553



Internal ID15850978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101881728..101942496hg38UCSC Ensembl
Outerchr15:101877403..101946203hg38UCSC Ensembl
Innerchr15:102421931..102482699hg19UCSC Ensembl
Outerchr15:102417606..102486406hg19UCSC Ensembl
Innerchr15:100239454..100300222hg18UCSC Ensembl
Outerchr15:100235129..100303929hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3868801
hg1968801
hg1868801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626178
Samples1
Known GenesOR4F4
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511553
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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