A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551416



Internal ID16338825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67186747..67346614hg38UCSC Ensembl
Innerchr10:68946505..69106372hg19UCSC Ensembl
Innerchr10:68616511..68776378hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38159868
hg19159868
hg18159868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174235
Samples1780854477_A
Known GenesCTNNA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551416
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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