A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599799



Internal ID6986844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18774723..18786518hg38UCSC Ensembl
chr4:18776346..18788141hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3811796
hg1911796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11363670, essv11363669
SamplesHG00351, HG01628
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599799
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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