A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619561



Internal ID7006435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10647445..10706472hg38UCSC Ensembl
chr9:10647445..10706472hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3859028
hg1959028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1441e214
Supporting Variantsessv13402186, essv13402187, essv13402185
SamplesHG00250, HG00131, HG00274
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619561
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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