A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635291



Internal ID6675404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89173999..89176052hg38UCSC Ensembl
Innerchr14:89174001..89176051hg38UCSC Ensembl
Outerchr14:89173998..89176054hg38UCSC Ensembl
chr14:89640343..89642396hg19UCSC Ensembl
Innerchr14:89640345..89642395hg19UCSC Ensembl
Outerchr14:89640342..89642398hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg382054
hg192054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15093023, essv15093021, essv15093018, essv15093019, essv15093022, essv15093024, essv15093020
SamplesNA20897, NA20845, HG03928, HG02737, HG02688, HG03718, HG03937
Known GenesFOXN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635291
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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