A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633367



Internal ID7020176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101768791..101806664hg38UCSC Ensembl
Innerchr13:101768813..101806642hg38UCSC Ensembl
Outerchr13:101768769..101806686hg38UCSC Ensembl
chr13:102421141..102459014hg19UCSC Ensembl
Innerchr13:102421163..102458992hg19UCSC Ensembl
Outerchr13:102421119..102459036hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3837874
hg1937874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14880840
SamplesHG00276
Known GenesFGF14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633367
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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