A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6518886



Internal ID8861639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109545263..109610390hg38UCSC Ensembl
Outerchr13:109545226..109610440hg38UCSC Ensembl
Innerchr13:110197610..110262737hg19UCSC Ensembl
Outerchr13:110197573..110262787hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3865215
hg1965215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668415
Supporting Variants
SamplesHG00318
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6518886
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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