A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619586



Internal ID7006460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11152893..11276567hg38UCSC Ensembl
chr9:11152893..11276567hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38123675
hg19123675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13402682, essv13402685, essv13402681, essv13402687, essv13402684, essv13402683, essv13402686
SamplesNA19350, NA18988, HG01513, NA19456, NA19321, NA19473, NA19435
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619586
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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