A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673382



Internal ID9939487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106857682..106865756hg38UCSC Ensembl
chr13:107510030..107518104hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg388075
hg198075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5774489, essv6483326
SamplesHG01070, HG00732
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673382
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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