A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7841834



Internal ID15083377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4183709..4183710hg38UCSC Ensembl
Innerchr10:4183693..4183726hg38UCSC Ensembl
Outerchr10:4183692..4183727hg38UCSC Ensembl
chr10:4225901..4225902hg19UCSC Ensembl
Innerchr10:4225885..4225918hg19UCSC Ensembl
Outerchr10:4225884..4225919hg19UCSC Ensembl
chr10:4215901..4215902hg18UCSC Ensembl
Innerchr10:4215918..4215885hg18UCSC Ensembl
Outerchr10:4215884..4215919hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38249
hg19249
hg18249
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308603
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7841834
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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