A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3975n54



Internal ID22771870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105124547..105167162hg38UCSC Ensembl
chr14:105590884..105633499hg19UCSC Ensembl
chr14:104661929..104704544hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3842616
hg1942616
hg1842616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566154, nsv566155
Samples1780862585_A
Known GenesJAG2, MIR6765
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3975n54
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