A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618229



Internal ID7005112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102590141..102594257hg38UCSC Ensembl
Innerchr8:102590191..102594207hg38UCSC Ensembl
Outerchr8:102590091..102594307hg38UCSC Ensembl
chr8:103602369..103606485hg19UCSC Ensembl
Innerchr8:103602419..103606435hg19UCSC Ensembl
Outerchr8:103602319..103606535hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg384117
hg194117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13270935
SamplesHG03057
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618229
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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