A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037793



Internal ID19127012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65517853..66063168hg38UCSC Ensembl
Innerchr10:67277611..67822926hg19UCSC Ensembl
Innerchr10:66947617..67492932hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38545316
hg19545316
hg18545316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504298
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037793
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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