A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552616



Internal ID16340025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133291695..133293066hg38UCSC Ensembl
Innerchr10:135105199..135106570hg19UCSC Ensembl
Innerchr10:134955189..134956560hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381372
hg191372
hg181372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv762556
Samples
Known GenesTUBGCP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552616
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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