A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5826242



Internal ID8803645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96267536..96273569hg38UCSC Ensembl
Outerchr13:96267379..96273722hg38UCSC Ensembl
Innerchr13:96919790..96925823hg19UCSC Ensembl
Outerchr13:96919633..96925976hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg386344
hg196344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669413
Supporting Variants
SamplesNA19190
Known GenesHS6ST3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5826242
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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