A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527578



Internal ID15108185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81191395..81778657hg38UCSC Ensembl
Innerchr11:80902438..81489699hg19UCSC Ensembl
Innerchr11:80580086..81167347hg18UCSC Ensembl
Innerchr11:80580086..81167347hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38587263
hg19587262
hg18587262
hg17587262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704039
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527578
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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