A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617782



Internal ID7004667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80595084..80596130hg38UCSC Ensembl
Innerchr8:80595134..80596080hg38UCSC Ensembl
Outerchr8:80594997..80596217hg38UCSC Ensembl
chr8:81507319..81508365hg19UCSC Ensembl
Innerchr8:81507369..81508315hg19UCSC Ensembl
Outerchr8:81507232..81508452hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381047
hg191047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13239036
SamplesHG03854
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617782
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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