A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551951



Internal ID16339360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94402684..94403492hg38UCSC Ensembl
Innerchr10:96162441..96163249hg19UCSC Ensembl
Innerchr10:96152431..96153239hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38809
hg19809
hg18809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1354n54
Supporting Variantsnssv755885
Samples
Known GenesTBC1D12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer