A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5669282



Internal ID9131755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68302685..68303243hg38UCSC Ensembl
Outerchr13:68302648..68303293hg38UCSC Ensembl
Innerchr13:68876817..68877375hg19UCSC Ensembl
Outerchr13:68876780..68877425hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658145
Supporting Variants
SamplesHG01171
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5669282
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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