A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603406



Internal ID16390815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64861877..65002395hg38UCSC Ensembl
Innerchr6:65571770..65712288hg19UCSC Ensembl
Innerchr6:65628491..65769009hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38140519
hg19140519
hg18140519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1062522
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603406
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