A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633192



Internal ID7020002
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv362e214
Supporting Variantsessv14861115, essv14861116, essv14861113, essv14861114, essv14861111, essv14861109, essv14861108, essv14861112, essv14861110
SamplesHG02652, HG03963, HG04182, HG03978, HG03888, HG03814, HG04235, HG04200, HG03809
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633192
Frequency
Sample Size2504
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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