A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516542



Internal ID15443835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78742600..78751770hg38UCSC Ensembl
Innerchr11:78453645..78462815hg19UCSC Ensembl
Innerchr11:78131293..78140463hg18UCSC Ensembl
Innerchr11:78131293..78140463hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg389171
hg199171
hg189171
hg179171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681211, nssv669008, nssv691998
Samples
Known GenesTENM4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516542
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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