A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3415696



Internal ID15262655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90693950..90694848hg38UCSC Ensembl
Innerchr9:90693949..90694849hg38UCSC Ensembl
Outerchr9:90692950..90695848hg38UCSC Ensembl
chr9:93456232..93457130hg19UCSC Ensembl
Innerchr9:93456231..93457131hg19UCSC Ensembl
Outerchr9:93455232..93458130hg19UCSC Ensembl
chr9:92496052..92496950hg18UCSC Ensembl
Innerchr9:92496951..92496051hg18UCSC Ensembl
Outerchr9:92495052..92497950hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697422
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3415696
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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