A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618139



Internal ID7005022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97550111..97555063hg38UCSC Ensembl
Innerchr8:97550111..97555063hg38UCSC Ensembl
Outerchr8:97549818..97555378hg38UCSC Ensembl
chr8:98562339..98567291hg19UCSC Ensembl
Innerchr8:98562339..98567291hg19UCSC Ensembl
Outerchr8:98562046..98567606hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg384953
hg194953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13267216
SamplesHG00672
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618139
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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