A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515484



Internal ID15443331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76143191..76151527hg38UCSC Ensembl
Innerchr11:75854235..75862571hg19UCSC Ensembl
Innerchr11:75531883..75540219hg18UCSC Ensembl
Innerchr11:75531883..75540219hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg388337
hg198337
hg188337
hg178337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673866, nssv651663
Samples
Known GenesUVRAG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515484
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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