A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7841714



Internal ID15083163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89826797..89826798hg38UCSC Ensembl
Innerchr9:89826780..89826815hg38UCSC Ensembl
Outerchr9:89826779..89826816hg38UCSC Ensembl
chr9:92528244..92528245hg19UCSC Ensembl
Innerchr9:92528227..92528262hg19UCSC Ensembl
Outerchr9:92528226..92528263hg19UCSC Ensembl
chr9:91668064..91668065hg18UCSC Ensembl
Innerchr9:91668082..91668047hg18UCSC Ensembl
Outerchr9:91668046..91668083hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38173
hg19173
hg18173
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3309751
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7841714
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