A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865400



Internal ID13317756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92798699..92798717hg38UCSC Ensembl
Innerchr10:92798669..92798747hg38UCSC Ensembl
Outerchr10:92798651..92798765hg38UCSC Ensembl
chr10:94558456..94558474hg19UCSC Ensembl
Innerchr10:94558426..94558504hg19UCSC Ensembl
Outerchr10:94558408..94558522hg19UCSC Ensembl
chr10:94548436..94548454hg18UCSC Ensembl
Innerchr10:94548484..94548406hg18UCSC Ensembl
Outerchr10:94548388..94548502hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3449838
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865400
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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