A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622513



Internal ID6662683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18605251..18653373hg38UCSC Ensembl
Innerchr10:18605251..18653373hg38UCSC Ensembl
Outerchr10:18604751..18653873hg38UCSC Ensembl
chr10:18894180..18942302hg19UCSC Ensembl
Innerchr10:18894180..18942302hg19UCSC Ensembl
Outerchr10:18893680..18942802hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3848123
hg1948123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13710225
SamplesHG03790
Known GenesNSUN6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622513
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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