A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602911



Internal ID16043634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35489619..35497706hg38UCSC Ensembl
Innerchr6:35457396..35465483hg19UCSC Ensembl
Innerchr6:35565374..35573461hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg388088
hg198088
hg188088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10624n54
Supporting Variantsnssv1058200
Samples
Known GenesTEAD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602911
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