A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551412



Internal ID16338821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66982272..66999167hg38UCSC Ensembl
Innerchr10:68742030..68758925hg19UCSC Ensembl
Innerchr10:68412036..68428931hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3816896
hg1916896
hg1816896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv749928
Samples
Known GenesCTNNA3, LRRTM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551412
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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