A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635295



Internal ID6675408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89461292..89471150hg38UCSC Ensembl
Innerchr14:89461292..89471150hg38UCSC Ensembl
Outerchr14:89460792..89471650hg38UCSC Ensembl
chr14:89927636..89937494hg19UCSC Ensembl
Innerchr14:89927636..89937494hg19UCSC Ensembl
Outerchr14:89927136..89937994hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg389859
hg199859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15093033, essv15093032, essv15093034
SamplesNA20811, NA20818, HG00236
Known GenesFOXN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635295
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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