A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618926



Internal ID7005808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135687431..135695818hg38UCSC Ensembl
Innerchr8:135687449..135695801hg38UCSC Ensembl
Outerchr8:135687414..135695836hg38UCSC Ensembl
chr8:136699674..136708061hg19UCSC Ensembl
Innerchr8:136699692..136708044hg19UCSC Ensembl
Outerchr8:136699657..136708079hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg388388
hg198388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13339105, essv13339106, essv13339107
SamplesHG00693, HG01797, HG00478
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618926
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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