A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635296



Internal ID6675409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89523871..89528912hg38UCSC Ensembl
Innerchr14:89524371..89528412hg38UCSC Ensembl
Outerchr14:89522871..89529912hg38UCSC Ensembl
chr14:89990215..89995256hg19UCSC Ensembl
Innerchr14:89990715..89994756hg19UCSC Ensembl
Outerchr14:89989215..89996256hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg385042
hg195042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15093036, essv15093037, essv15093039, essv15093035, essv15093038
SamplesHG02727, HG03779, HG03792, HG03875, NA21105
Known GenesFOXN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635296
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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