A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677887



Internal ID9943992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45584922..45589233hg38UCSC Ensembl
Outerchr21:45584885..45589283hg38UCSC Ensembl
Innerchr21:47004836..47009147hg19UCSC Ensembl
Outerchr21:47004799..47009197hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg384399
hg194399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6006314
SamplesHG00663
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677887
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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