A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5909892



Internal ID8915647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104349487..104352848hg38UCSC Ensembl
chr13:105001837..105005198hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg383362
hg193362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678212
Supporting Variants
SamplesHG00418
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5909892
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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