A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3385412



Internal ID15232382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92036689..92036695hg38UCSC Ensembl
Innerchr10:92036674..92036710hg38UCSC Ensembl
Outerchr10:92036668..92036716hg38UCSC Ensembl
chr10:93796446..93796452hg19UCSC Ensembl
Innerchr10:93796431..93796467hg19UCSC Ensembl
Outerchr10:93796425..93796473hg19UCSC Ensembl
chr10:93786426..93786432hg18UCSC Ensembl
Innerchr10:93786447..93786411hg18UCSC Ensembl
Outerchr10:93786405..93786453hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865399
SamplesNA18516
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3385412
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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