A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15092059



Internal ID3255462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87141202..87165457hg38UCSC Ensembl
chr14:87607546..87631801hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3824256
hg1924256
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635251
Supporting Variants
SamplesHG02879
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15092059
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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