A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525450



Internal ID15452743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115516731..115542275hg38UCSC Ensembl
Innerchr11:115387449..115412993hg19UCSC Ensembl
Innerchr11:114892659..114918203hg18UCSC Ensembl
Innerchr11:114892659..114918203hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3825545
hg1925545
hg1825545
hg1725545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701578
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525450
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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