A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555170



Internal ID15995893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61492279..61612174hg38UCSC Ensembl
Innerchr11:61259751..61379646hg19UCSC Ensembl
Innerchr11:61016327..61136222hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38119896
hg19119896
hg18119896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1962n54
Supporting Variantsnssv777137
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)nsv555170
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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