A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15117402



Internal ID365984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105079623..105114221hg38UCSC Ensembl
chr14:105545960..105580558hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3834599
hg1934599
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635637
Supporting Variants
SamplesHG00105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15117402
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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