A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602966



Internal ID16390375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40523539..40556231hg38UCSC Ensembl
Innerchr6:40491278..40523970hg19UCSC Ensembl
Innerchr6:40599256..40631948hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3832693
hg1932693
hg1832693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058393
Samples
Known GenesLRFN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602966
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