A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552316



Internal ID16339725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129945867..130029486hg38UCSC Ensembl
Innerchr10:131744131..131827750hg19UCSC Ensembl
Innerchr10:131634121..131717740hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3883620
hg1983620
hg1883620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760798
Samples
Known GenesEBF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552316
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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