A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621690



Internal ID7008557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123297636..123307842hg38UCSC Ensembl
Innerchr9:123297786..123307692hg38UCSC Ensembl
Outerchr9:123297486..123307992hg38UCSC Ensembl
chr9:126059915..126070121hg19UCSC Ensembl
Innerchr9:126060065..126069971hg19UCSC Ensembl
Outerchr9:126059765..126070271hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3810207
hg1910207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618441
SamplesNA19984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621690
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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