A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3308093



Internal ID15155041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17699961..17699962hg38UCSC Ensembl
Innerchr9:17699797..17700126hg38UCSC Ensembl
Outerchr9:17699796..17700127hg38UCSC Ensembl
chr9:17699959..17699960hg19UCSC Ensembl
Innerchr9:17699795..17700124hg19UCSC Ensembl
Outerchr9:17699794..17700125hg19UCSC Ensembl
chr9:17689959..17689960hg18UCSC Ensembl
Innerchr9:17690124..17689795hg18UCSC Ensembl
Outerchr9:17689794..17690125hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3881
hg1981
hg1881
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7837687, essv7837053
SamplesNA19239, NA19240
Known GenesSH3GL2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3308093
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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