A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595657



Internal ID6635931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26983690..27173105hg38UCSC Ensembl
chr3:27025181..27214596hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38189416
hg19189416
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv880e214
Supporting Variantsessv10961117, essv10961116
SamplesHG03369, NA20334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595657
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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