A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519857



Internal ID15100464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117653828..117654161hg38UCSC Ensembl
Innerchr11:117524543..117524876hg19UCSC Ensembl
Innerchr11:117029753..117030086hg18UCSC Ensembl
Innerchr11:117029753..117030086hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38334
hg19334
hg18334
hg17334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685899, nssv693183, nssv678904, nssv659111
Samples
Known GenesDSCAML1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519857
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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