A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645685



Internal ID7032434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33586659..33597547hg38UCSC Ensembl
Innerchr20:33586659..33597547hg38UCSC Ensembl
Outerchr20:33586413..33597833hg38UCSC Ensembl
chr20:32174465..32185353hg19UCSC Ensembl
Innerchr20:32174465..32185353hg19UCSC Ensembl
Outerchr20:32174219..32185639hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3810889
hg1910889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16175544, essv16175546, essv16175545, essv16175547
SamplesHG01802, HG02407, HG03833, NA18636
Known GenesCBFA2T2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645685
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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