A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14861109



Internal ID4236106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93163177..93201452hg38UCSC Ensembl
chr13:93815430..93853705hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3838276
hg1938276
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633192
Supporting Variants
SamplesHG03809
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14861109
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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