A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16299967



Internal ID4678832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26407645..26413300hg38UCSC Ensembl
Innerchr21:26407645..26413300hg38UCSC Ensembl
Outerchr21:26407377..26413549hg38UCSC Ensembl
chr21:27779964..27785619hg19UCSC Ensembl
Innerchr21:27779964..27785619hg19UCSC Ensembl
Outerchr21:27779696..27785868hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg385656
hg195656
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3646733
Supporting Variants
SamplesHG04202
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16299967
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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