A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619806



Internal ID7006680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16068892..16098796hg38UCSC Ensembl
chr9:16068890..16098794hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3829905
hg1929905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1455e214
Supporting Variantsessv13410062, essv13410061
SamplesHG02070, NA18981
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619806
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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