A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8671806



Internal ID15105038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4183710..4183716hg38UCSC Ensembl
Innerchr10:4183702..4183724hg38UCSC Ensembl
Outerchr10:4183694..4183730hg38UCSC Ensembl
chr10:4225902..4225908hg19UCSC Ensembl
Innerchr10:4225894..4225916hg19UCSC Ensembl
Outerchr10:4225886..4225922hg19UCSC Ensembl
chr10:4215902..4215908hg18UCSC Ensembl
Innerchr10:4215916..4215894hg18UCSC Ensembl
Outerchr10:4215886..4215922hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38239
hg19239
hg18239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3325142
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8671806
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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