A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646287



Internal ID7033032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62228081..62229147hg38UCSC Ensembl
Innerchr20:62228123..62229106hg38UCSC Ensembl
Outerchr20:62228040..62229189hg38UCSC Ensembl
chr20:60803137..60804203hg19UCSC Ensembl
Innerchr20:60803179..60804162hg19UCSC Ensembl
Outerchr20:60803096..60804245hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381067
hg191067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16221003
SamplesNA20858
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646287
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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