A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8949966



Internal ID14518689
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 StatusS
Merged Variantsesv3392688
Supporting Variants
SamplesNA19114
Known GenesR3HCC1L
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8949966
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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