A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599284



Internal ID6986332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196441634..196463645hg38UCSC Ensembl
chr3:196168505..196190516hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3822012
hg1922012
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11308386, essv11308387, essv11308385
SamplesHG03559, HG02079, HG02410
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599284
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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