A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13710223



Internal ID3712039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18550373..18655215hg38UCSC Ensembl
chr10:18839302..18944144hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38104843
hg19104843
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622511
Supporting Variants
SamplesHG03790
Known GenesNSUN6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13710223
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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