A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645439



Internal ID6685501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18475870..18486400hg38UCSC Ensembl
Innerchr20:18475870..18486400hg38UCSC Ensembl
Outerchr20:18475370..18486900hg38UCSC Ensembl
chr20:18456514..18467044hg19UCSC Ensembl
Innerchr20:18456514..18467044hg19UCSC Ensembl
Outerchr20:18456014..18467544hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3810531
hg1910531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16154863
SamplesNA20587
Known GenesPOLR3F
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645439
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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