A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551789



Internal ID15992512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86655261..86668319hg38UCSC Ensembl
Innerchr10:88415018..88428076hg19UCSC Ensembl
Innerchr10:88404998..88418056hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3813059
hg1913059
hg1813059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1320n54
Supporting Variantsnssv752230
Samples
Known GenesOPN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551789
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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