A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551950



Internal ID16339359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94402684..94403387hg38UCSC Ensembl
Innerchr10:96162441..96163144hg19UCSC Ensembl
Innerchr10:96152431..96153134hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38704
hg19704
hg18704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv755884
Samples
Known GenesTBC1D12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551950
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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