A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601489



Internal ID16388898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31092385..31114584hg38UCSC Ensembl
Innerchr6:31060162..31082361hg19UCSC Ensembl
Innerchr6:31168141..31190340hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3822200
hg1922200
hg1822200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1052286
Samples
Known GenesC6orf15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601489
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