A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645484



Internal ID7032233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20756251..20760537hg38UCSC Ensembl
Innerchr20:20756251..20760537hg38UCSC Ensembl
Outerchr20:20756051..20760703hg38UCSC Ensembl
chr20:20736894..20741180hg19UCSC Ensembl
Innerchr20:20736894..20741180hg19UCSC Ensembl
Outerchr20:20736694..20741346hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384287
hg194287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16155725, essv16155724
SamplesNA19075, NA18910
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645484
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer