A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635258



Internal ID7022057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87349605..87351444hg38UCSC Ensembl
Innerchr14:87349624..87351426hg38UCSC Ensembl
Outerchr14:87349587..87351463hg38UCSC Ensembl
chr14:87815949..87817788hg19UCSC Ensembl
Innerchr14:87815968..87817770hg19UCSC Ensembl
Outerchr14:87815931..87817807hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg381840
hg191840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15092069
SamplesHG02721
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635258
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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