A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5124n54



Internal ID22773019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54378967..54385662hg38UCSC Ensembl
chr16:54412879..54419574hg19UCSC Ensembl
chr16:52970380..52977075hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg386696
hg196696
hg186696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572625, nsv572626, nsv572628, nsv572624
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5124n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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