A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617860



Internal ID7004744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84522461..84524946hg38UCSC Ensembl
Innerchr8:84522490..84524917hg38UCSC Ensembl
Outerchr8:84522432..84524975hg38UCSC Ensembl
chr8:85434696..85437181hg19UCSC Ensembl
Innerchr8:85434725..85437152hg19UCSC Ensembl
Outerchr8:85434667..85437210hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg382486
hg192486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13244284
SamplesHG02786
Known GenesRALYL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617860
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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