A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646899



Internal ID7033641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32959296..32966419hg38UCSC Ensembl
Innerchr21:32959303..32966412hg38UCSC Ensembl
Outerchr21:32959289..32966426hg38UCSC Ensembl
chr21:34331604..34338727hg19UCSC Ensembl
Innerchr21:34331611..34338720hg19UCSC Ensembl
Outerchr21:34331597..34338734hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg387124
hg197124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16313554
SamplesHG03731
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646899
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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