A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6137632



Internal ID8943852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109799359..109812501hg38UCSC Ensembl
Outerchr13:109799322..109812551hg38UCSC Ensembl
Innerchr13:110451706..110464848hg19UCSC Ensembl
Outerchr13:110451669..110464898hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3813230
hg1913230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663610
Supporting Variants
SamplesHG00475
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6137632
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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