A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555737



Internal ID15996460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89179523..89538618hg38UCSC Ensembl
Innerchr11:88912691..89271786hg19UCSC Ensembl
Innerchr11:88552339..88911434hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38359096
hg19359096
hg18359096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2062n54
Supporting Variantsnssv1176198
SamplesHGDP00664
Known GenesNOX4, TYR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555737
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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