A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612862



Internal ID16400271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143616728..143632493hg38UCSC Ensembl
Innerchr8:144698898..144714663hg19UCSC Ensembl
Innerchr8:144770041..144785806hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3815766
hg1915766
hg1815766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12427n54
Supporting Variantsnssv1125574
Samples
Known GenesTSTA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612862
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