A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635192



Internal ID6675305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85476603..85687645hg38UCSC Ensembl
chr14:85942947..86153989hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38211043
hg19211043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15089613
SamplesNA06984
Known GenesFLRT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635192
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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