A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551794



Internal ID15992517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86660172..86662359hg38UCSC Ensembl
Innerchr10:88419929..88422116hg19UCSC Ensembl
Innerchr10:88409909..88412096hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382188
hg192188
hg182188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752235, nssv752234
Samples
Known GenesOPN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551794
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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