A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612853



Internal ID16053576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143616727..143626978hg38UCSC Ensembl
Innerchr8:144698897..144709148hg19UCSC Ensembl
Innerchr8:144770040..144780291hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3810252
hg1910252
hg1810252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12428n54
Supporting Variantsnssv1125561
Samples
Known GenesTSTA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612853
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