A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634027



Internal ID7020831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34369105..34373456hg38UCSC Ensembl
chr14:34838311..34842662hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg384352
hg194352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv391e214
Supporting Variantsessv14965029
SamplesNA19334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634027
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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