A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3392688



Internal ID14892967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98137958..98138000hg38UCSC Ensembl
Innerchr10:98137976..98137979hg38UCSC Ensembl
Outerchr10:98137940..98138018hg38UCSC Ensembl
chr10:99897715..99897757hg19UCSC Ensembl
Innerchr10:99897733..99897736hg19UCSC Ensembl
Outerchr10:99897697..99897775hg19UCSC Ensembl
chr10:99887705..99887747hg18UCSC Ensembl
Innerchr10:99887723..99887726hg18UCSC Ensembl
Outerchr10:99887687..99887765hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3892
hg1992
hg1892
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8949967, essv8949968, essv8949966
SamplesNA19114, NA18505, NA18853
Known GenesR3HCC1L
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3392688
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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