A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616935



Internal ID7003821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38903921..38908617hg38UCSC Ensembl
Innerchr8:38903977..38908562hg38UCSC Ensembl
Outerchr8:38903866..38908673hg38UCSC Ensembl
chr8:38761439..38766135hg19UCSC Ensembl
Innerchr8:38761495..38766080hg19UCSC Ensembl
Outerchr8:38761384..38766191hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg384697
hg194697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13169177
SamplesHG00476
Known GenesPLEKHA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616935
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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