A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9643625



Internal ID13368604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72480397..72480416hg38UCSC Ensembl
Innerchr9:72480393..72480420hg38UCSC Ensembl
Outerchr9:72480374..72480439hg38UCSC Ensembl
chr9:75095313..75095332hg19UCSC Ensembl
Innerchr9:75095309..75095336hg19UCSC Ensembl
Outerchr9:75095290..75095355hg19UCSC Ensembl
chr9:74285133..74285152hg18UCSC Ensembl
Innerchr9:74285156..74285129hg18UCSC Ensembl
Outerchr9:74285110..74285175hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg386000
hg196000
hg186000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3427927
Supporting Variants
SamplesNA12045
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9643625
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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