A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551786



Internal ID16339195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86654460..86661284hg38UCSC Ensembl
Innerchr10:88414217..88421041hg19UCSC Ensembl
Innerchr10:88404197..88411021hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg386825
hg196825
hg186825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1322n54
Supporting Variantsnssv752227
Samples
Known GenesOPN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551786
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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