A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634409



Internal ID7021212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47259738..47283588hg38UCSC Ensembl
chr14:47728941..47752791hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3823851
hg1923851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv400e214
Supporting Variantsessv15003287, essv15003286
SamplesHG03558, HG03069
Known GenesMDGA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634409
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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