A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1071956



Internal ID15925142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108559544..108561634hg38UCSC Ensembl
Innerchr6:108880747..108882837hg19UCSC Ensembl
Innerchr6:108987440..108989530hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382091
hg192091
hg182091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604479
Supporting Variants
Samples
Known GenesFOXO3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1071956
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