A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15089868



Internal ID6604890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85852484..85900162hg38UCSC Ensembl
chr14:86318828..86366506hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3847679
hg1947679
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635211
Supporting Variants
SamplesNA20773
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15089868
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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