A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618295



Internal ID7005177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105926959..105929535hg38UCSC Ensembl
Innerchr8:105926980..105929514hg38UCSC Ensembl
Outerchr8:105926938..105929556hg38UCSC Ensembl
chr8:106939187..106941763hg19UCSC Ensembl
Innerchr8:106939208..106941742hg19UCSC Ensembl
Outerchr8:106939166..106941784hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg382577
hg192577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13275072
SamplesHG00099
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618295
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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