A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634026



Internal ID7020830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34369096..34374792hg38UCSC Ensembl
Innerchr14:34369596..34374292hg38UCSC Ensembl
Outerchr14:34368096..34375792hg38UCSC Ensembl
chr14:34838302..34843998hg19UCSC Ensembl
Innerchr14:34838802..34843498hg19UCSC Ensembl
Outerchr14:34837302..34844998hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg385697
hg195697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv391e214
Supporting Variantsessv14965028
SamplesNA19334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634026
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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