A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8687989



Internal ID15007883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133777937..133787422hg38UCSC Ensembl
Innerchr10:133778937..133786435hg38UCSC Ensembl
Outerchr10:133776937..133787422hg38UCSC Ensembl
chr10:135515262..135524747hg19UCSC Ensembl
Innerchr10:135516262..135523760hg19UCSC Ensembl
Outerchr10:135514262..135524747hg19UCSC Ensembl
chr10:135365252..135374737hg18UCSC Ensembl
Innerchr10:135366252..135373750hg18UCSC Ensembl
Outerchr10:135364252..135374737hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg389486
hg199486
hg189486
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3327924
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8687989
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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