A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551411



Internal ID15992134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66923058..66961819hg38UCSC Ensembl
Innerchr10:68682816..68721577hg19UCSC Ensembl
Innerchr10:68352822..68391583hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3838762
hg1938762
hg1838762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174234
Samples1780862003_A
Known GenesCTNNA3, LRRTM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551411
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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