A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635593



Internal ID6675706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103377962..103437655hg38UCSC Ensembl
chr14:103844299..103903992hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3859694
hg1959694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv422e214
Supporting Variantsessv15114329, essv15114328
SamplesNA06984, HG00598
Known GenesMARK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635593
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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