A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1662n54



Internal ID18993838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16185112..16245194hg38UCSC Ensembl
chr11:16206658..16266740hg19UCSC Ensembl
chr11:16163234..16223316hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3860083
hg1960083
hg1860083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553564, nsv553563
Samples1780862001_A
Known GenesSOX6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1662n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer