A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616891



Internal ID7003777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35943561..35953271hg38UCSC Ensembl
Innerchr8:35943595..35953237hg38UCSC Ensembl
Outerchr8:35943527..35953305hg38UCSC Ensembl
chr8:35801079..35810789hg19UCSC Ensembl
Innerchr8:35801113..35810755hg19UCSC Ensembl
Outerchr8:35801045..35810823hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389711
hg199711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13167941
SamplesHG01122
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616891
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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