A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7742656



Internal ID14665331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97258579..97258580hg38UCSC Ensembl
Innerchr8:97258542..97258617hg38UCSC Ensembl
Outerchr8:97258541..97258618hg38UCSC Ensembl
chr8:98270807..98270808hg19UCSC Ensembl
Innerchr8:98270770..98270845hg19UCSC Ensembl
Outerchr8:98270769..98270846hg19UCSC Ensembl
chr8:98339983..98339984hg18UCSC Ensembl
Innerchr8:98340021..98339946hg18UCSC Ensembl
Outerchr8:98339945..98340022hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38256
hg19256
hg18256
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307729
Supporting Variants
SamplesNA18964
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7742656
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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