A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634818



Internal ID7021618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68204307..68210803hg38UCSC Ensembl
Innerchr14:68204307..68210803hg38UCSC Ensembl
Outerchr14:68203807..68211303hg38UCSC Ensembl
chr14:68671024..68677520hg19UCSC Ensembl
Innerchr14:68671024..68677520hg19UCSC Ensembl
Outerchr14:68670524..68678020hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg386497
hg196497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15048443
SamplesNA18908
Known GenesRAD51B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634818
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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