A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555736



Internal ID15996459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89179523..89535343hg38UCSC Ensembl
Innerchr11:88912691..89268511hg19UCSC Ensembl
Innerchr11:88552339..88908159hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38355821
hg19355821
hg18355821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2062n54
Supporting Variantsnssv1176197
SamplesHGDP00978
Known GenesNOX4, TYR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555736
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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