A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7769158



Internal ID13364963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72480406..72480407hg38UCSC Ensembl
Innerchr9:72480384..72480429hg38UCSC Ensembl
Outerchr9:72480383..72480430hg38UCSC Ensembl
chr9:75095322..75095323hg19UCSC Ensembl
Innerchr9:75095300..75095345hg19UCSC Ensembl
Outerchr9:75095299..75095346hg19UCSC Ensembl
chr9:74285142..74285143hg18UCSC Ensembl
Innerchr9:74285165..74285120hg18UCSC Ensembl
Outerchr9:74285119..74285166hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38441
hg19441
hg18441
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3306017
Supporting Variants
SamplesNA12045
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7769158
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer