A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673618



Internal ID9939723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15157390..15159634hg38UCSC Ensembl
chr9:15157388..15159632hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382245
hg192245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1328e199
Supporting Variantsessv6003652, essv5673412, essv6043241, essv6406517, essv5964484, essv6239214, essv6098668, essv6521970, essv5718244, essv6352890, essv6450987, essv5673573, essv5922738, essv5758826, essv6577780, essv5686486
SamplesNA19190, NA19374, NA19384, NA19371, NA19901, NA18867, HG01124, NA19462, NA19982, NA18910, HG01390, NA18517, NA19835, NA19360, NA18501, NA19430
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673618
Frequency
Sample Size1151
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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