A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688106



Internal ID14693765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46283210..46300008hg38UCSC Ensembl
Innerchr10:46284210..46299008hg38UCSC Ensembl
Outerchr10:46282210..46301008hg38UCSC Ensembl
chr10:47654446..47671244hg19UCSC Ensembl
Innerchr10:47655446..47670244hg19UCSC Ensembl
Outerchr10:47653446..47672244hg19UCSC Ensembl
chr10:47124452..47141250hg18UCSC Ensembl
Innerchr10:47125452..47140250hg18UCSC Ensembl
Outerchr10:47123452..47142250hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3816799
hg1916799
hg1816799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3439446
Supporting Variants
SamplesNA19239
Known GenesANTXRL
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688106
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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