A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511151



Internal ID15850576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158898012..158899943hg38UCSC Ensembl
Outerchr1:158885764..158901663hg38UCSC Ensembl
Innerchr1:158867802..158869733hg19UCSC Ensembl
Outerchr1:158855554..158871453hg19UCSC Ensembl
Innerchr1:157134426..157136357hg18UCSC Ensembl
Outerchr1:157122178..157138077hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3815900
hg1915900
hg1815900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626010
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511151
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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