A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645454



Internal ID7032204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19200289..19201330hg38UCSC Ensembl
Innerchr20:19200337..19201283hg38UCSC Ensembl
Outerchr20:19200242..19201378hg38UCSC Ensembl
chr20:19180933..19181974hg19UCSC Ensembl
Innerchr20:19180981..19181927hg19UCSC Ensembl
Outerchr20:19180886..19182022hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16154999, essv16155017, essv16155016, essv16155023, essv16155018, essv16155019, essv16155024, essv16155005, essv16155006, essv16155001, essv16155010, essv16155013, essv16154998, essv16155015, essv16155020, essv16155021, essv16155011, essv16155004, essv16155014, essv16155000, essv16155003, essv16155007, essv16155012, essv16155002, essv16155022, essv16155009, essv16155008
SamplesHG02890, NA19141, HG03558, HG03577, HG03095, NA19374, HG02952, HG03209, NA18874, NA19189, HG03073, HG03583, HG02334, HG02450, NA20126, HG02878, HG02979, NA19225, HG02799, NA19712, HG02721, HG02923, HG03469, HG03433, NA19472, NA19102, HG02284
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645454
Frequency
Sample Size2504
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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