A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635571



Internal ID6675684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102772846..102911700hg38UCSC Ensembl
chr14:103239183..103378037hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38138855
hg19138855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15109992, essv15109991, essv15109993, essv15109994
SamplesHG00304, HG00369, HG00368, NA06984
Known GenesTRAF3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635571
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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