A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647026



Internal ID6687082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39723451..39731234hg38UCSC Ensembl
Innerchr21:39723462..39731223hg38UCSC Ensembl
Outerchr21:39723440..39731245hg38UCSC Ensembl
chr21:41095378..41103161hg19UCSC Ensembl
Innerchr21:41095389..41103150hg19UCSC Ensembl
Outerchr21:41095367..41103172hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg387784
hg197784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16320988
SamplesNA19060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647026
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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