A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051902



Internal ID19141121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67576984..67677150hg38UCSC Ensembl
Innerchr10:69336742..69436908hg19UCSC Ensembl
Innerchr10:69006748..69106914hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38100167
hg19100167
hg18100167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv917n100
Supporting Variantsnssv3521854
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)nsv1051902
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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