A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3649n54



Internal ID22771544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38489763..38605974hg38UCSC Ensembl
chr14:38958967..39075178hg19UCSC Ensembl
chr14:38028718..38144929hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38116212
hg19116212
hg18116212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564415, nsv564414
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3649n54
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