A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599699



Internal ID6986744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13259639..13289412hg38UCSC Ensembl
chr4:13261263..13291036hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3829774
hg1929774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11359156, essv11359154, essv11359155
SamplesNA18986, NA18605, HG01864
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599699
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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