A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5518065



Internal ID8495468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96206879..96208310hg38UCSC Ensembl
chr13:96859133..96860564hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381432
hg191432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2673647
Supporting Variants
SamplesNA19404
Known GenesHS6ST3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5518065
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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