A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15092058



Internal ID3255468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87137837..87165053hg38UCSC Ensembl
Innerchr14:87138337..87164553hg38UCSC Ensembl
Outerchr14:87136837..87166053hg38UCSC Ensembl
chr14:87604181..87631397hg19UCSC Ensembl
Innerchr14:87604681..87630897hg19UCSC Ensembl
Outerchr14:87603181..87632397hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3827217
hg1927217
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635250
Supporting Variants
SamplesHG02879
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15092058
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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