A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552745



Internal ID16340154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133566995..133634467hg38UCSC Ensembl
Innerchr10:135380499..135447971hg19UCSC Ensembl
Innerchr10:135230489..135297961hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3867473
hg1967473
hg1867473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1497n54
Supporting Variantsnssv763021
Samples
Known GenesFRG2B, SPRNP1, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552745
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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