A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046118



Internal ID19135337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67514918..67544382hg38UCSC Ensembl
Innerchr10:69274676..69304140hg19UCSC Ensembl
Innerchr10:68944682..68974146hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3829465
hg1929465
hg1829465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517780
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)nsv1046118
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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