A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619587



Internal ID7006461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11152893..11276567hg38UCSC Ensembl
chr9:11152893..11276567hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38123675
hg19123675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13402689, essv13402688
SamplesNA20274, NA19625
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619587
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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