A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5526666



Internal ID8767783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103875640..103881795hg38UCSC Ensembl
chr13:104527990..104534145hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg386156
hg196156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665487
Supporting Variants
SamplesHG00159
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5526666
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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