A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13093751



Internal ID3893827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8978882..8979585hg38UCSC Ensembl
Innerchr8:8978882..8979585hg38UCSC Ensembl
Outerchr8:8978678..8979825hg38UCSC Ensembl
chr8:8836392..8837095hg19UCSC Ensembl
Innerchr8:8836392..8837095hg19UCSC Ensembl
Outerchr8:8836188..8837335hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616161
Supporting Variants
SamplesHG03548
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13093751
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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