A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555168



Internal ID15995891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61492279..61536331hg38UCSC Ensembl
Innerchr11:61259751..61303803hg19UCSC Ensembl
Innerchr11:61016327..61060379hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3844053
hg1944053
hg1844053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777135, nssv777136
Samples
Known GenesLRRC10B, MIR4488, SYT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555168
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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