A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633281



Internal ID6673403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96838169..96838762hg38UCSC Ensembl
Innerchr13:96838169..96838762hg38UCSC Ensembl
Outerchr13:96837890..96839019hg38UCSC Ensembl
chr13:97490423..97491016hg19UCSC Ensembl
Innerchr13:97490423..97491016hg19UCSC Ensembl
Outerchr13:97490144..97491273hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14869341, essv14869342
SamplesHG00188, HG00339
Known GenesHS6ST3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633281
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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