A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646734



Internal ID7033477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26409516..26412629hg38UCSC Ensembl
Innerchr21:26409547..26412599hg38UCSC Ensembl
Outerchr21:26409486..26412660hg38UCSC Ensembl
chr21:27781835..27784948hg19UCSC Ensembl
Innerchr21:27781866..27784918hg19UCSC Ensembl
Outerchr21:27781805..27784979hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg383114
hg193114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16299968
SamplesNA18537
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646734
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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