A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511486



Internal ID15850911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45408851..45409855hg38UCSC Ensembl
Outerchr11:45407831..45416824hg38UCSC Ensembl
Innerchr11:45430401..45431405hg19UCSC Ensembl
Outerchr11:45429381..45438374hg19UCSC Ensembl
Innerchr11:45386977..45387981hg18UCSC Ensembl
Outerchr11:45385957..45394950hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg388994
hg198994
hg188994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626103
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)nsv511486
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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