A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153394



Internal ID15876208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:284613..381217hg38UCSC Ensembl
Innerchr6:284613..381217hg19UCSC Ensembl
Innerchr6:229613..326217hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3896605
hg1996605
hg1896605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600762
Supporting Variants
SamplesHGDP00801
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153394
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