A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616914



Internal ID6657110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38051747..38056815hg38UCSC Ensembl
Innerchr8:38051811..38056751hg38UCSC Ensembl
Outerchr8:38051683..38056879hg38UCSC Ensembl
chr8:37909265..37914333hg19UCSC Ensembl
Innerchr8:37909329..37914269hg19UCSC Ensembl
Outerchr8:37909201..37914397hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385069
hg195069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13169015
SamplesNA19090
Known GenesEIF4EBP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616914
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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