A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616783



Internal ID7003669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30039160..30048616hg38UCSC Ensembl
Innerchr8:30039660..30048116hg38UCSC Ensembl
Outerchr8:30038160..30049616hg38UCSC Ensembl
chr8:29896676..29906132hg19UCSC Ensembl
Innerchr8:29897176..29905632hg19UCSC Ensembl
Outerchr8:29895676..29907132hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389457
hg199457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13154927
SamplesHG04026
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616783
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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