A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617690



Internal ID7004575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75847476..75876784hg38UCSC Ensembl
Innerchr8:75847498..75876763hg38UCSC Ensembl
Outerchr8:75847455..75876806hg38UCSC Ensembl
chr8:76759711..76789019hg19UCSC Ensembl
Innerchr8:76759733..76788998hg19UCSC Ensembl
Outerchr8:76759690..76789041hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3829309
hg1929309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13234746
SamplesHG00362
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617690
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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