A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645503



Internal ID7032252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22344810..22349612hg38UCSC Ensembl
Innerchr20:22344819..22349603hg38UCSC Ensembl
Outerchr20:22344801..22349621hg38UCSC Ensembl
chr20:22325448..22330250hg19UCSC Ensembl
Innerchr20:22325457..22330241hg19UCSC Ensembl
Outerchr20:22325439..22330259hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg384803
hg194803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16160043, essv16160049, essv16160042, essv16160052, essv16160050, essv16160046, essv16160040, essv16160044, essv16160053, essv16160048, essv16160041, essv16160047, essv16160045, essv16160051
SamplesNA20339, HG02804, HG03464, HG02111, NA19923, NA19172, HG02588, HG03267, NA20127, HG02477, HG02582, NA18853, NA19160, HG02484
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645503
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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