A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3713n54



Internal ID22771608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48819161..48902680hg38UCSC Ensembl
chr14:49288364..49371883hg19UCSC Ensembl
chr14:48358114..48441633hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3883520
hg1983520
hg1883520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564829, nsv564831
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3713n54
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