A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632837



Internal ID7019648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80458912..80481975hg38UCSC Ensembl
chr13:81033047..81056110hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3823064
hg1923064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv353e214
Supporting Variantsessv14814722
SamplesHG00632
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632837
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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