A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618320



Internal ID7005202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106876590..106883497hg38UCSC Ensembl
Innerchr8:106876590..106883497hg38UCSC Ensembl
Outerchr8:106876090..106883997hg38UCSC Ensembl
chr8:107888818..107895725hg19UCSC Ensembl
Innerchr8:107888818..107895725hg19UCSC Ensembl
Outerchr8:107888318..107896225hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg386908
hg196908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13278896
SamplesHG02307
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618320
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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