A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603441



Internal ID16390850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65436926..65522799hg38UCSC Ensembl
Innerchr6:66146819..66232692hg19UCSC Ensembl
Innerchr6:66203540..66289413hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3885874
hg1985874
hg1885874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10727n54
Supporting Variantsnssv1153710
SamplesHGDP00146
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603441
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