A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633539



Internal ID7020348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110080127..110109124hg38UCSC Ensembl
chr13:110732474..110761471hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3828998
hg1928998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv371e214
Supporting Variantsessv14895749, essv14895750, essv14895748, essv14895753, essv14895754, essv14895751, essv14895755, essv14895752
SamplesHG01051, HG00641, HG01067, HG01673, HG01187, HG01190, HG01086, HG01105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633539
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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