A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1734n54



Internal ID22769629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31369686..31375622hg38UCSC Ensembl
chr11:31391233..31397169hg19UCSC Ensembl
chr11:31347809..31353745hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385937
hg195937
hg185937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553953, nsv553952, nsv553951
Samples
Known GenesDCDC1, DNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1734n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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