A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5848065



Internal ID9438284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18624734..18634871hg38UCSC Ensembl
chr10:18913663..18923800hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3810138
hg1910138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670942
Supporting Variants
SamplesNA18637
Known GenesNSUN6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5848065
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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