A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963087



Internal ID16257043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52056328..52062416hg38UCSC Ensembl
Innerchr3:52090344..52096432hg19UCSC Ensembl
Innerchr3:52065384..52071472hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg386089
hg196089
hg186089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590299
Supporting Variants
Samples
Known GenesDUSP7, LINC00696
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963087
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